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Fresenius Medical Care AG & Co. KGaA

Quarterly Report Aug 31, 2010

165_10-q_2010-08-31_508caf29-d207-43d2-a3ca-297c4d08c9ba.pdf

Quarterly Report

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Q2/ 2010

Fresenius Medical Care

overview page 3

Interim Report of Management's Discussion and Analysis page 7 Financial Condition and Results of Operations page 7 Liquidity and Capital Resources page 20 Balance Sheet Structure page 25 Outlook page 25 Recently Issued Accounting Standards page 25

Consolidated Financial Statements page 26

Consolidated Statements of Income page 26 Consolidated Statements of Comprehensive Income page 27 Consolidated Balance Sheets page 28 Consolidated Statements of Cash Flows page 29 Consolidated Statements of Shareholders´ Equity page 30 Notes to Consolidated Financial Statements page 32

Events occurring after the balance sheet daTE page 51

Corporate Governance page 51

responsibility statement page 51

Calendar and Contact page 52

overview

second Quarter 2010 Summ
ary
Table 1
Net revenue \$ 2,946 million + 7 %
Operating income (EBIT) \$ 465 million + 11 %
Net income1 \$ 248 million + 12 %
Earnings per share \$ 0.83 + 12 %
First half 2010 Summ
ary
Table 2
Net revenue \$ 5,828 million + 9 %
Operating income (EBIT) \$ 888 million + 9 %
Net income1 \$ 459 million + 10 %
Earnings per share \$ 1.53 + 9 %

Net income attributable to Fresenius Medical Care AG & Co. KGaA

second quarter 2010

Revenue

Net revenue for the second quarter of 2010 increased by 7 % to \$ 2,946 million (also + 7 % at constant currency) compared to the second quarter of 2009. Organic revenue growth worldwide was 6 %. Dialysis services revenue grew by 8 % to \$ 2,224 million (also + 8 % at constant currency) in the second quarter of 2010. Dialysis product revenue rose by 2 % to \$ 722 million (+ 3 % at constant currency) in the same period.

North America revenue increased by 8 % to \$ 2,027 million. Organic revenue growth was 7 %. Dialysis services revenue grew by 8 % to \$ 1,817 million. Average revenue per treatment for U.S. clinics increased to \$ 356 in the second quarter of 2010 compared to \$ 344 for the same quarter in 2009 and \$ 355 for the first quarter of 2010. This development was attributable principally to reimbursement increases and increased utilization of pharmaceuticals. Dialysis product revenue increased by 5 % to \$ 210 million due to higher sales of hemodialysis disposables and dialysis machines.

International revenue increased by 4 % to \$ 919 million. Based on constant currency, revenue grew by 5 %. Organic revenue growth was 3 %. Dialysis services revenue was \$ 407 million, an increase of 8 % (+ 9 % at constant currency). Dialysis product revenue was stable at \$ 512 million compared to the corresponding figure last year and increased by 2 % at constant currency, led by increased sales of hemodialysis solutions and concentrates, dialyzers and bloodlines as well as products for acute care treatment.

Earnings

Operating income ( EBIT ) increased by 11 % to \$ 465 million compared to \$ 418 million in the second quarter of 2009 resulting in an operating margin of 15.8 % compared to 15.1 % for the corresponding quarter in 2009.

In North America, the operating margin increased from 15.9 % to 16.3 % in the second quarter of 2010. The margin development was mainly impacted favorably by an increase in revenue per treatment as well as the effect of economies of scale from revenue growth.

In the International segment, the operating margin increased from 17.3 % to 18.8 %. The margin development was mainly influenced positively by economies of scale from revenue growth, favorable foreign exchange rates and lower bad debt expenses. This was partially offset by higher depreciation expenses as a result of the expansion of our production capacities.

Net interest expense for the second quarter of 2010 was \$ 68 million compared to \$ 76 million in the comparable quarter of 2009, mainly attributable to lower short-term interest rates.

Income tax expense was \$ 129 million for the second quarter of 2010 compared to \$ 103 million in the second quarter of 2009, reflecting effective tax rates of 32.6 % and 30.2 %, respectively. In both the second quarter of 2010 and 2009 tax expense benefited from changes in estimates of future tax payments.

Net income attributable to FMC AG & Co. KGaA for the second quarter of 2010 was \$ 248 million, an increase of 12 % compared to the same quarter of 2009.

Earnings per share ( EPS ) for the second quarter of 2010 rose by 12 % to \$ 0.83 per ordinary share compared to \$ 0.74 for the second quarter of 2009. The weighted average number of shares outstanding for the second quarter of 2010 was approximately 300.0 million shares compared to 298.0 million shares for the second quarter of 2009. The increase in shares outstanding resulted from stock option exercises in the past twelve months.

Cash Flow In the second quarter of 2010, the Company generated \$ 294 million in cash from operations, representing approximately 10 % of revenue. The cash flow performance was influenced positively by improvements in elements of working capital and increased earnings, partially offset by higher income tax payments.

A total of \$ 119 million was spent for capital expenditures, net of disposals. Free cash flow before acquisitions was \$ 175 million compared to \$ 143 million in the second quarter of 2009. A total of \$ 68 million in cash was spent for acquisitions, net of divestitures. Free cash flow after acquisitions and divestitures was \$ 107 million compared to \$ 98 million in the second quarter of last year.

first half of 2010

Revenue and Earnings

Net revenue was \$ 5,828 million, up 9 % from the first half of 2009. At constant currency, net revenue rose 8 %. Organic growth was 7 % in the first six months of 2010.

Operating income ( EBIT ) increased by 9 % to \$ 888 million compared to \$ 813 million in the first half of 2009, resulting in an operating margin of 15.2 % compared to 15.3 % for the first half of 2009.

Net interest expense for the first six months of 2010 was \$ 135 million compared to \$ 149 million in the same period of 2009.

Income tax expense was \$ 257 million in the first half of 2010 compared to \$ 214 million in the same period in 2009, reflecting effective tax rates of 34.1 % and 32.2 %, respectively.

For the first half of 2010, net income attributable to FMC AG & Co. KGaA was \$ 459 million, up 10 % from the first half of 2009.

In the first six months of 2010, earnings per ordinary share rose 9 % to \$ 1.53. The weighted average number of shares outstanding during the first half of 2010 was approximately 299.8 million.

Cash Flow

Cash from operations during the first six months of 2010 was \$ 643 million compared to \$ 437 million for the same period in 2009, representing approximately 11 % of revenue.

A total of \$ 218 million was spent for capital expenditures, net of disposals. Free Cash Flow before acquisitions for the first six months of 2010 was \$ 425 million compared to \$ 188 million in the same period in 2009. A total of \$ 150 million in cash was spent for acquisitions, net of divestitures. Free Cash Flow after acquisitions and divestitures was \$ 275 million compared to \$ 107 million in the first half of last year.

Patients – Clinics – Treatments As of June 30, 2010, Fresenius Medical Care treated 202,414 patients worldwide, which represents a 6 % increase compared to the previous year. North America provided dialysis treatments for 135,088 patients, the number of patients treated rose by 5 %. Including 29 clinics managed by Fresenius Medical Care North America, the number of patients in North America was 136,884. The International segment served 67,326 patients, the number of patients treated increased by 11 %.

As of June 30, 2010, the Company operated a total of 2,599 clinics worldwide, which represents a 5 % increase compared to the previous year. The number of clinics is comprised of 1,795 clinics in North America (1,824 including managed clinics) and 804 clinics in the International segment, representing an increase of 4 % and 9 %, respectively.

Fresenius Medical Care delivered approximately 15.26 million dialysis treatments worldwide during the first six months of 2010. This represents an increase of 6 % compared to the corresponding period last year. North America accounted for 10.22 million treatments, an increase of 6 %, and the International segment delivered 5.03 million treatments, an increase of 8 %.

Employees As of June 30, 2010, Fresenius Medical Care had 70,096 employees (full-time equivalents) worldwide compared to 67,988 employees at the end of 2009. The increase of approximately 2,100 employees is due to overall growth in the Company's business.

Debt/EBITDA Ratio The ratio of debt to Earnings before Interest, Taxes, Depreciation and Amortization ( EBITDA ) decreased from 2.78 at the end of the second quarter of 2009 to 2.46 at the end of the second quarter 2010. At the end of 2009, the debt / EBITDA ratio was 2.46.

Rating Standard & Poor's Rating Services continued to rate the Company's corporate credit as 'BB'. On April 29, 2010, Standard & Poor's has raised the outlook from 'stable' to 'positive'. Moody's continued to rate the Company's corporate credit as 'Ba1' with a 'stable' outlook. Fitch rates the Company's corporate credit as 'BB' also with a 'stable' outlook. For further information on Fresenius Medical Care's credit ratings, maturity profiles and credit instruments, please visit our website at www.fmc-ag.com / Investor Relations/ Credit Relations.

Outlook for 2010 fully confirmed For the full year of 2010, the Company confirms its outlook.

Revenue is expected to grow to more than \$ 12 billion.

Net income attributable to FMC AG & Co. KGaA is expected to be between \$ 950 million and \$ 980 million in 2010.

The Company expects to spend \$ 550 million to \$ 650 million on capital expenditures and up to \$ 500 million (previously up to \$ 400 million) on acquisitions. The debt/ EBITDA ratio is expected to be below 2.5 by the end of 2010.

Interim Report of Management's Discussion and Analysis

Financial Condition and Results of Operations You should read the following discussion and analysis of the results of operations of Fresenius Medical Care AG & Co. KGaA (FMC-AG & Co. KGaA, or the Company) and its subsidiaries in conjunction with our unaudited consolidated financial statements and related notes contained elsewhere in this report and our disclosures and discussions in our Annual Report on Form 20-F for the year ended December 31, 2009. In this report, "FMC-AG & Co. KGaA" or the "Company", "we", "us" or "our" refers to the Company or the Company and its subsidiaries on a consolidated basis, as the context requires.

Forward-looking Statements This report contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. When used in this report, the words "expects", "anticipates", "intends", "plans", "believes", "seeks", "estimates" and similar expressions are generally intended to identify forward looking statements. Although we believe that the expectations reflected in such forward-looking statements are reasonable, forward-looking statements are inherently subject to risks and uncertainties, many of which cannot be predicted with accuracy and some of which might not even be anticipated. We have based these forwardlooking statements on current estimates and assumptions made to the best of our knowledge. By their nature, such forward-looking statements involve risks, uncertainties, assumptions and other factors which could cause actual results, including our financial condition and profitability, to differ materially and be more negative than the results expressly or implicitly described in or suggested by these statements. Moreover, forward-looking estimates or predictions derived from third parties' studies or information may prove to be inaccurate. Consequently, we cannot give any assurance regarding the future accuracy of the opinions set forth in this report or the actual occurrence of the developments described herein. In addition, even if our future results meet the expectations expressed here, those results may not be indicative of our performance in future periods.

These risks, uncertainties, assumptions, and other factors that could cause actual results to differ from our projected results include, among others, the following:

  • changes in governmental and commercial insurer reimbursement for our products and services, including the mandated change in the United States beginning in 2011 to an expanded "bundled" Medicare reimbursement system for dialysis services;
  • reductions in erythropoietin, or EPO, utilization or EPO reimbursement;
  • the outcome of ongoing government investigations;
  • the influence of private insurers and managed care organizations;
  • the impact of recently enacted and possible future health care reforms;
  • product liability risks;
  • the outcome of ongoing potentially material litigation;
  • risks relating to the integration of acquisitions and our dependence on additional acquisitions;
  • the impact of currency fluctuations;
  • changes in the cost of pharmaceuticals and utilization patterns;
  • introduction of generic or new pharmaceuticals that compete with our pharmaceutical products;
  • changes in raw material and energy costs; and
  • other statements of our expectations, beliefs, future plans and strategies, anticipated development and other matters that are not historical facts.

Important factors that could contribute to such differences are noted in this report in the section entitled "Interim Report of Management's Discussion and Analysis" and in Note 9 "Commitments and Contingencies" and in our Annual Report on Form 20-F for the year ended December 31, 2009 under "Risk Factors" and elsewhere in that report.

Our business is also subject to other risks and uncertainties that we describe from time to time in our public filings. Developments in any of these areas could cause our results to differ materially from the results that we or others have projected or may project.

Our reported financial condition and results of operations are sensitive to accounting methods, assumptions and estimates that are the basis of our financial statements. The actual accounting policies, the judgments made in the selection and application of these policies, and the sensitivities of reported results to changes in accounting policies, assumptions and estimates, are factors to be considered along with our financial statements and the discussion below under "Results of Operations". For a discussion of our critical accounting policies  see Item 5 "Operating and Financial Review and Prospects – Critical Accounting Policies" in our Annual Report on Form 20-F for the year ended December 31, 2009.

Overview We are engaged primarily in providing dialysis services and manufacturing and distributing products and equipment for the treatment of end-stage renal disease ( ESRD ). In the U.S., we also perform clinical laboratory testing. We estimate that providing dialysis services and distributing dialysis products and equipment represents an over \$ 65 billion worldwide market with expected annual worldwide patient growth of around 6 %. Patient growth results from factors such as the aging population and increased life expectancies; shortage of donor organs for kidney transplants, increasing incidence and better treatment of and survival of patients with diabetes and hypertension, which frequently precede the onset of ESRD; improvements in treatment quality, which prolong patient life; and improving standards of living in developing countries, which make life-saving dialysis treatment available. Key to continued growth in revenue is our ability to attract new patients in order to increase the number of treatments performed each year. For that reason, we believe the number of treatments performed each year is a strong indicator of continued revenue growth and success. In addition, the reimbursement and ancillary services utilization environment significantly influences our business. In the past we experienced and also expect in the future generally stable reimbursements for dialysis services. This includes the balancing of unfavorable reimbursement changes in certain countries with favorable changes in other countries. The majority of treatments are paid for by governmental institutions such as Medicare in the United States. As a consequence of the pressure to decrease health care costs, reimbursement rate increases have been limited. Our ability to influence the pricing of our services is limited. Profitability depends on our ability to manage rising labor, drug and supply costs.

A majority of our U.S. dialysis services are paid for by the Medicare program. Medicare payments for dialysis services are based on a composite rate which includes a drug add-on adjustment, case-mix adjustments, and a regional wage index adjustment. The drug add-on adjustment was established under the Medicare Prescription Drug, Improvement and Modernization Act of 2003 (MMA) to account for differences in Medicare reimbursement for separately billable pharmaceuticals pre-MMA and the new average sales price reimbursement system established by the MMA.

For calendar year 2010, the Centers for Medicare and Medicaid Services (CMS) kept the drug add-on amount constant at the 2009 rate of \$ 20.33 per treatment, while it increased the base portion of the composite rate by 1 % pursuant to the requirement in the Medicare Improvements for Patients and Providers Act of 2008 (MIPPA). As a result, the drug add-on amount, constant in dollar terms, declined to 15 % of the total pertreatment payment in 2010. The base portion of the composite rate, unlike many other payment rates in Medicare, has not been automatically updated each year. As a result, this portion of the composite payment rate has not received an annual update in the absence of a statutory change. In MIPPA, Congress provided for a 1.0 % increase in the base portion of the composite rate in 2010. Further, Congress eliminated a provision that previously paid hospital-based facilities slightly more than independent (or free-standing) facilities. For 2010, the base composite rate is \$ 135.15 for both independent and hospital-based facilities, an increase of 1.0 % from the 2009 rate. CMS updated the wage index adjustment applicable to ESRD facilities from the 25/75

blend between adjustments based on old metropolitan statistical areas (MSAs) and those based on new corebased statistical areas (CBSAs) used in 2008. In 2009, CMS completed the transition from the MSA definition to the CBSA definition, and facilities are now paid according to the CBSA rate. For 2010, CMS reduced the wage index floor from 0.70 to 0.65. For a discussion of the composite rate for reimbursement of dialysis treatments,  see Item 4.B "Business Overview – Regulatory and Legal Matters – Reimbursement" in our Annual Report on Form 20-F for the year ended December 31, 2009.

Certain other items and services that we furnish at our dialysis centers are not now included in the composite rate and are eligible for separate Medicare reimbursement. The most significant of these items are drugs or biologicals, such as erythropoietin-stimulating agents (ESAs), vitamin D analogs, and iron, which are reimbursed at 106 % of the average sales price as reported to CMS by the manufacturer. Products and support services furnished to ESRD patients receiving dialysis treatment at home are also reimbursed separately under a reimbursement structure comparable to the in-center composite rate. Although these reimbursement methodologies limit the allowable charge per treatment, they provide us with predictable per treatment revenues.

With the enactment of MIPPA in 2008, Congress mandated the development of an expanded ESRD bundled payment system for services furnished on or after January 1, 2011. On July 26, 2010, CMS published a final rule implementing the case-mix adjusted bundled prospective payment system (PPS) for ESRD dialysis facilities in accordance with MIPPA. Under the PPS, CMS will reimburse dialysis facilities with a single payment for each dialysis treatment, inclusive of (i) all items and services included in the composite rate, (ii) oral vitamin D analogues, oral levocarnitine (an amino acid derivative) and all ESAs and other pharmaceuticals (other than vaccines) furnished to ESRD patients that were previously reimbursed separately under Part B of the Medicare program, (iii) certain diagnostic laboratory tests and (iv) other items and services furnished to individuals for the treatment of ESRD. ESRD-related drugs with only an oral form will be reimbursed under the PPS starting in January 2014 with an adjusted payment amount to be determined by the Secretary of Health and Human Services to reflect the additional cost to dialysis facilities of providing these medications. The initial PPS base reimbursement rate will be set at \$ 229.63 per dialysis treatment. The base PPS payment will be subject to case mix adjustments that take into account individual patient characteristics (e.g., age, body surface area, body mass, time on dialysis) and certain co-morbidities. The base payment will also be adjusted for (i) certain high cost patient outliers due to unusual variations in medically necessary care, (ii) disparately high costs incurred by low volume facilities relative to other facilities, (iii) provision of home dialysis training, (iv) wagerelated costs in the geographic area in which the provider is located and (v) blending of the old and new payment methodologies during the phase in of the new system. Beginning in 2012, the PPS payment amount will be subject to annual adjustment based on increases in the costs of a "market basket" of certain dialysis items and services minus 1 %. The PPS's pay-for-performance standards, focusing on anemia management and dialysis adequacy, will become effective in 2012. Dialysis facilities that fail to achieve the established quality standards will have payments reduced by up to 2 %. The PPS will be phased in over four years with full implementation for all dialysis facilities on January 1, 2014. However, providers may elect in November 2010 to become fully subject to the new system starting in January 2011. We are currently evaluating the impact of PPS on our business and whether we will become fully subject to the PPS starting in January 2011 or phase PPS in over the allowable four year period.

The Patient Protection and Affordable Care Act was enacted in the United States on March 23, 2010 and subsequently amended by the Health Care and Educational Affordability Reconciliation Act (as amended, PPACA). PPACA will implement broad healthcare system reforms, including (i) provisions to facilitate access to affordable health insurance for all Americans, (ii) expansion of the Medicaid program, (iii) an industry fee on

pharmaceutical companies starting in 2011 based on sales of brand name pharmaceuticals to government healthcare programs, (iv) a 2.3 % excise tax on manufacturers' medical device sales starting in 2013, (v) increases in Medicaid prescription drug rebates effective January 1, 2010, (vi) commercial insurance market reforms that protect consumers, such as bans on lifetime and annual limits, coverage of pre-existing conditions, and limits on waiting periods, (vii) provisions encouraging integrated care, efficiency and coordination among providers and (viii) provisions for reduction of healthcare program waste and fraud. PPACA does not modify the dialysis reimbursement provisions of MIPPA. PPACA's medical device excise tax, Medicaid drug rebate increases and annual pharmaceutical industry fees will adversely impact our product business earnings and cash flows. We expect modest favorable impact from PPACA's integrated care and commercial insurance consumer protection provisions.

On February 17, 2010, the Department of Veterans Affairs (VA) issued proposed reimbursement rules that would reduce its payment rates for non-contracted dialysis services to coincide with those of the Medicare program. If the proposed rules are implemented as currently proposed, we expect to experience variability in our aggregated VA reimbursement rates for contracted and non-contracted services. In addition, we may also experience reductions in the volume of VA patients treated in our facilities.

We have identified three operating segments, North America, International, and Asia Pacific. For reporting purposes, we have aggregated the International and Asia Pacific segments as "International". We aggregated these segments due to their similar economic characteristics. These characteristics include same services provided and same products sold, same type patient population, similar methods of distribution of products and services and similar economic environments. The general partner's Management Board member responsible for the profitability and cash flow of each segment's various businesses supervises the management of each operating segment. The accounting policies of the operating segments are the same as those we apply in preparing our consolidated financial statements under accounting principles generally accepted in the United States (U.S. GAAP). Our management evaluates each segment using a measure that reflects all of the segment's controllable revenues and expenses.

With respect to the performance of our business operations, our management believes the most appropriate measure in this regard is operating income which measures our source of earnings. Financing is a corporate function which segments do not control. Therefore, we do not include interest expense relating to financing as a segment measurement. We also regard income taxes to be outside the segments' control. Similarly, we do not allocate "corporate costs", which relate primarily to certain headquarters overhead charges, including accounting and finance, professional services, etc. because we believe that these costs are also not within the control of the individual segments. In addition, certain acquisitions and intangible assets are not allocated to a segment but are accounted for as "corporate". Accordingly, all of these items are excluded from our analysis of segment results and are discussed below in the discussion of our consolidated results of operations.

Results of Operations The following tables summarize our financial performance and certain operating results by principal business segment for the periods indicated. Inter-segment sales primarily reflect sales of medical equipment and supplies from the International segment to the North America segment. We prepared

the information using a management approach, consistent with the basis and manner in which our management internally disaggregates financial information to assist in making internal operating decisions and evaluating management performance.

segment data
in \$ millions Table 3
Three months ended June 30, Six months ended June 30,
2010 2009 2010 2009
Total revenue
North America 2,028 1,877 3,988 3,651
International 941 909 1,885 1,712
Total 2,969 2,786 5,873 5,363
Inter-segment revenue
North America 1 1 2 1
International 22 21 43 39
Total 23 22 45 40
Total net revenue
North America 2,027 1,876 3,986 3,650
International 919 888 1,842 1,673
Total 2,946 2,764 5,828 5,323
Amortization and depreciation
North America 71 65 143 129
International 47 43 98 83
Corporate 3 2 5 4
Total 121 110 246 216
Operating income
North America 330 297 636 569
International 173 154 324 300
Corporate (38) (33) (72) (56)
Total 465 418 888 813
Interest income 8 7 14 12
Interest expense (76) (83) (149) (161)
Income tax expense (129) (103) (257) (214)
Net income 268 239 496 450
Less: Net income attributable to noncontrolling interests 20 18 37 31
net income1 248 221 459 419

Net income attributable to FMC-AG & Co. KGaA

Three months ended June 30, 2010 compared to three months ended June 30, 2009.

Consolidated Financials

Key Indicators for Consolidated Financial Statements Table 4
Three months ended June 30, Change
2010 2009 as reported at constant
exchange rates
Number of treatments 7,749,584 7,314,822 6 %
Same market treatment growth in % 4.3 4.3
Revenue in \$ millions 2,946 2,764 7 % 7 %
Gross profit in % of revenue 34.3 33.7
Selling, general and administrative costs in % of revenue 17.8 17.9
Net income1 in \$ millions 248 221 12 %

1 Net income attributable to FMC-AG & Co. KGaA

We provided 7,749,584 treatments during the second quarter of 2010, an increase of 6 % over the same period in 2009. Same market treatment growth contributed 4 %, and growth from acquisitions contributed 2 %.

At June 30, 2010, we owned, operated or managed (excluding those managed but not consolidated in the U.S.) 2,599 clinics compared to 2,471 clinics at June 30, 2009. During the second quarter of 2010, we acquired 9 clinics, opened 27 clinics and combined or closed 17 clinics. The number of patients treated in clinics that we own, operate or manage (excluding patients of clinics managed but not consolidated in the U.S.) increased by 6 % to 202,414 at June 30, 2010 from 190,081 at June 30, 2009. Including 29 clinics managed but not consolidated in the U.S., the total number of patients was 204,210.

Net revenue increased by 7 % (7 % at constant exchange rates) for the quarter ended June 30, 2010 over the comparable period in 2009 due to growth in both dialysis care and dialysis products revenues.

Dialysis care revenue grew by 8 % to \$ 2,224 million (8 % at constant exchange rates) in the second quarter of 2010 as compared to the same period in 2009, mainly due to growth in same market treatments (4 %), increases in revenue per treatment (3 %), and contributions from acquisitions (2 %), partially offset by the effect of closed and sold clinics (1 %).

Dialysis product revenue increased by 2 % to \$ 722 million (increased by 3 % at constant exchange rates) in the same period driven by increased sales of hemodialysis products, especially of solutions and concentrates, bloodlines and dialyzers as well as products for acute care treatments.

The increase in gross profit margin reflects an increase in gross profit margin in North America, partially offset by a decrease in the International segment. The increase in North America was due to increased revenue per treatment and favorable costs for pharmaceuticals, partially offset by higher personnel expense. The decrease in International was due to a margin decrease in the Japan product business, a reimbursement reduction in Taiwan and increased depreciation expense related to the expansion of production capacities, partially offset by business growth in China.

Selling, general and administrative (SG&A) expenses increased to \$ 526 million in the second quarter of 2010 from \$ 495 million in the same period of 2009. SG&A expensese as a percentage of sales decreased to 17.8 % in the second quarter of 2010 from 17.9 % in the same period of 2009. SG&A expenses decreased in the International segment mainly due to economies of scale, foreign exchange currency gains and lower bad debt expense. SG&A expenses increased in North America due to higher personnel expenses and donations to U.S. ESRD patient assistance charities, partially offset by economies of scale. In addition, SG&A expenses increased at Corporate due to expenses related to patent litigations. Bad debt expense for the second quarter of 2010 was \$ 55 million as compared to \$ 56 million for the second quarter of 2009, representing 1.9 % of sales for the three-month period ending June 30, 2010 and 2.0 % for the same period in 2009.

Research and development (R&D) expenses increased to \$ 21 million in the second quarter of 2010 as compared to \$ 19 million in the same period of 2009.

Operating income increased to \$ 465 million in the second quarter of 2010 from \$ 418 million for the same period in 2009. Operating income margin increased to 15.8 % for the period ending June 30, 2010 from 15.1 % for the same period in 2009 as a result of the increase in gross profit margin as noted above as well as the decreased SG&A expenses as a percentage of sales as described above.

Interest expense decreased by 8 % to \$ 87 million in the second quarter of 2010 from \$ 83 million for the same period in 2009 mainly as a result of decreased short-term interest rates.

Income tax expense increased to \$ 129 million for the second quarter of 2010 from \$ 103 million for the same period in 2009. The effective tax rate increased to 32.6 % from 30.2 % for the second quarter of 2009. This was mainly due to the result of a \$ 16.3 million tax benefit recognized in the second quarter of 2009 as a result of a change in judgment related to a complaint filed with the German tax court on the disallowance of certain tax deductions we claimed for the tax year 1997, partially offset by the release of a \$ 10 million valuation allowance in the second quarter of 2010 on deferred taxes for net operating losses due to a change in tax strategies.

Net income attributable to FMC-AG & Co. KGaA for the second quarter of 2010 increased to \$ 248 million from \$ 221 million for the same period in 2009 as a result of the combined effects of the items discussed above.

We employed 70,096 people (full-time equivalents) as of June 30, 2010 compared to 66,364 as of June 30, 2009, an increase of 5.6 % primarily due to overall growth in our business.

The following discussions pertain to our business segments and the measures we use to manage these segments.

North America Segment

Key Indicators for North Am
Table 5
erica Segment
Three months ended June 30, Change
2010 2009
Number of treatments 5,189,159 4,945,148 5 %
Same market treatment growth in % 4.2 3.6
Revenue in \$ millions 2,027 1,876 8 %
Depreciation and amortization in \$ millions 71 65 10 %
Operating income in \$ millions 330 297 11 %
Operating income margin in % 16.3 15.9

Revenue Treatments increased by 5 % for the three-month period ended June 30, 2010 as compared to the same period in 2009 mostly due to same market growth (4 %) and contributions from acquisitions (1 %). At June 30, 2010, 135,088 patients (a 5 % increase over the same period in the prior year) were being treated in the 1,795 clinics that we own or operate in the North America segment, compared to 129,163 patients treated in 1,731 clinics at June 30, 2009. Average North America revenue per treatment was \$ 349 for the three months ended June 30, 2010 and \$ 338 in the same period in 2009. In the U.S., the average revenue per treatment was \$ 356 for the three months ended June 30, 2010 and \$ 344 for the same period in 2009. The increase was mainly attributable to increased commercial payor revenue and overall increased utilization of pharmaceuticals. Medicare had a minimal positive impact, as the effect of the 1 % increase in the 2010 Medicare composite rate was mostly offset by the effect of a decrease in reimbursement for pharmaceuticals.

Net revenue for the North America segment for the second quarter of 2010 increased as a result of increases in dialysis care revenue by 8 % to \$ 1,817 million from \$ 1,677 million in the same period of 2009 and in dialysis product revenue by 5 % to \$ 210 million from \$ 199 million in the second quarter of 2009.

The dialysis care revenue increase was driven by same market treatment growth (4 %), increased revenue per treatment (3 %) and contributions from acquisitions (2 %), partially offset by the effect of closed or sold clinics (1 %). The administration of EPO represented approximately 20 % of total North America dialysis care revenue for the three-month period ended June 30, 2010 and 21 % for the three-month period ended June 30, 2009.

The dialysis product revenue increase was driven mostly by increased sales of bloodlines, concentrates, dialyzers and machines.

Operating Income Operating income increased to \$ 330 million for the three-month period ended June 30, 2010 from \$ 297 million for the same period in 2009. Operating income margin increased to 16.3 % for the second quarter of 2010 from 15.9 % for the same period in 2009, primarily due to higher revenue per treatment, economies of scale and favorable costs for pharmaceuticals, partially offset by higher personnel expenses and donations to U.S. ESRD patient assistance charities. Cost per treatment increased to \$ 287 in the second quarter of 2010 from \$ 284 in the same period of 2009.

Key Indicators for International Segment
Table 6
Three months ended June 30, Change
2010 2009 as reported at constant
exchange rates
Number of treatments 2,560,425 2,369,674 8 %
Same market treatment growth in % 4.4 6.0
Revenue in \$ millions 919 888 4 % 5 %
Depreciation and amortization in \$ millions 47 43 9 %
Operating income in \$ millions 173 154 13 %
Operating income margin in % 18.8 17.3

International Segment

Revenue Treatments increased by 8 % in the three-month period ended June 30, 2010 over the same period in 2009 mainly due to same market growth of 4 % and contributions from acquisitions of 4 %. As of June 30, 2010, 67,326 patients (an 11 % increase over the same period of the prior year) were being treated at 804 clinics that we own, operate or manage in the International segment compared to 60,918 patients treated at 740 clinics at June 30, 2009. Average revenue per treatment remained constant at \$ 159. A net increase of \$ 1 resulted from increased reimbursement rates, partially offset by growth in countries with lower reimbursement rates. This net increase was offset by a \$ 1 decrease as a result of the weakening of local currencies against the U.S. dollar.

Net revenues for the International segment for the three-month period ended June 30, 2010 increased by 4 % (5 % increase at constant exchange rates) as compared to the same period in 2009 as a result of increases in both dialysis care and dialysis product revenues. Organic growth during the period was 3 % and acquisitions contributed approximately 2 %, partially offset by the negative effect of exchange rate fluctuations (1 %).

Including the effects of acquisitions, European region revenue decreased 1 % (4 % increase at constant exchange rates), Latin America region revenue increased 15 % (8 % increase at constant exchange rates), and Asia Pacific region revenue increased 12 % (5 % increase at constant exchange rates).

Total dialysis care revenue for the International segment increased during the second quarter of 2010 by 8 % (9 % increase at constant exchange rates) to \$ 407 million from \$ 377 million in the same period of 2009. This increase is a result of same market treatment growth (4 %), and increase in contributions from acquisitions (4 %) and the positive impact increases in revenue per treatment (1 %). Partially offsetting these increases was the negative effect of exchange rate fluctuations (1 %).

Total dialysis product revenue for the second quarter of 2010 increased slightly to \$ 512 million from \$ 510 million in the same period of 2009. The increase in product revenue was driven by increased sales of hemodialysis solutions and concentrates, dialyzers and bloodlines as well as products for acute care treatments. Organic revenue growth of 2 % was completely offset by the negative effect of exchange rate fluctuations of 2 %.

Operating Income Operating income increased by 13 % to \$ 173 million for the three-month period ended June 30, 2010 from \$ 154 million for the same period in 2009. Operating income margin increased to 18.8 % for the three-month period ended June 30, 2010 from 17.3 % for the same period in 2009 due to economies of scale, foreign exchange currency gains and lower bad debt expense, partially offset by a margin decrease in the Japan business, a reimbursement reduction in Taiwan and increased depreciation expense related to the expansion of production capacities.

Six months ended June 30, 2010 compared to six months ended June 30, 2009.

Consolidated Financials

Key Indicators for Consolidated Financial Statements Table 7
Six months ended June 30, Change
2010 2009 as reported at constant
exchange rates
Number of treatments 15,258,148 14,355,996 6 %
Same market treatment growth in % 4.3 4.4
Revenue in \$ millions 5,828 5,323 9 % 8 %
Gross profit in % of revenue 33.9 33.7
Selling, general and administrative costs in % of revenue 17.9 17.6
Net income1 in \$ millions 459 419 10 %

1 Net income attributable to FMC-AG & Co. KGaA

We provided 15,258,148 treatments during the six-month period ended June 30, 2010, an increase of 6 % over the same period in 2009. Same market treatment growth contributed 4 % and growth from acquisitions contributed 2 %.

Net revenue increased by 9 % (8 % at constant exchange rates) for the six months ended June 30, 2010 over the comparable period in 2009 due to growth in both dialysis care and dialysis products revenues.

Dialysis care revenue grew by 11 % to \$ 4,395 million (10 % at constant exchange rates) in the six-month period ended June 30, 2010 from \$ 3,977 million in the same period of 2009, mainly due to increases in revenue per treatment (4 %), growth in same market treatments (4 %), contributions from acquisitions (2 %), and the effect of additional treatments related to beginning of the year holiday scheduling in 2010 as compared to the same period in 2009 (1 %), as well as a positive effect from exchange rate fluctuations (1 %). These increases were partially offset by the effect of closed or sold clinics (1 %).

Dialysis product revenue increased by 6 % to \$ 1,433 million (increased by 4 % at constant exchange rates) from \$ 1,346 million in the same period of 2009, driven by increased sales of hemodialysis products, especially of solutions and concentrates, dialyzers and bloodlines as well as products for acute care treatments. Foreign exchange fluctuations contributed 2 %.

The increase in gross profit margin reflects an increase in gross profit margin in North America, partially offset by a decrease in the International segment. The increase in North America was due to increased revenue per treatment and favorable costs for pharmaceuticals, partially offset by higher personnel expense. The decrease in International was due to the positive effect of an inventory adjustment during the same period of 2009, a reimbursement cut in Taiwan and increased depreciation expense related to the expansion of production capacities partially offset by business growth in China.

Selling, general and administrative (SG&A) expenses increased to \$ 1,043 million in the six-month period ended June 30, 2010 from \$ 939 million in the same period of 2009. SG&A expenses as a percentage of sales increased to 17.9 % in the first six months of 2010 from 17.6 % in the same period of 2009 as a result of an increase in North America and at Corporate, partially offset by a decrease in the International segment. The increase in North America was due to higher personnel expenses and donations to U.S. ESRD patient assistance charities, partially offset by economies of scale, while the increase at Corporate was related to unfavorable foreign exchange currency effects and expenses related to patent litigations. The decrease in the International segment was mainly due to economies of scale and favorable foreign currency exchange gains, partially offset by the one-time revaluation of the balance sheet of our operations in Venezuela as a result of the devaluation of the Venezuelan bolivar driven by hyperinflation. Bad debt expense for the six-month period ended June 30, 2010 was \$ 116 million as compared to \$ 109 million for the same period of 2009, representing 2.0 % of sales for the six-month periods ended June 30, 2010 and 2009.

Research and development (R&D) expenses increased to \$ 44 million in the six-month period ended June 30, 2010 as compared to \$ 42 million in the same period in 2009.

Operating income increased to \$ 888 million in the six-month period ended June 30, 2010 from \$ 813 million for the same period in 2009. Operating income margin decreased slightly to 15.2 % for the six-month period ended June 30, 2010 from 15.3 % for the same period in 2009 as a result of increased SG&A expenses as a percentage of sales as described above partially offset by the increase in gross profit margin as noted above.

Interest expense decreased by 7 % to \$ 159 million for the six months ended June 30, 2010 from \$ 161 million for the same period in 2009 mainly as a result of decreased short-term interest rates.

Income tax expense increased to \$ 257 million for the six-month period ended June 30, 2010 from \$ 214 million for the same period in 2009. The effective tax rate increased to 34.1 % from 32.2 % for the same period of 2009. This was mainly due to the result of a \$ 16.3 million tax benefit recognized in the second quarter of 2009 as a result of a change in judgment related to a complaint filed with the German tax court on the disallowance of certain tax deductions claimed by us for the tax year 1997, partially offset by the release of a \$ 10 million valuation allowance in the second quarter of 2010 on deferred taxes for net operating losses due to a change in tax strategies.

Net income attributable to FMC-AG & Co. KGaA for the six months ended June 30, 2010 increased to \$ 459 million from \$ 419 million for the same period in 2009 as a result of the combined effects of the items discussed above.

The following discussions pertain to our business segments and the measures we use to manage these segments.

North America Segment

Key Indicators for North Am
Table 8
erica Segment
Six months ended June 30, Change
2010 2009
Number of treatments 10,223,675 9,689,699 6 %
Same market treatment growth in % 4.2 3.4
Revenue in \$ millions 3,986 3,650 9 %
Depreciation and amortization in \$ millions 143 129 11 %
Operating income in \$ millions 636 569 12 %
Operating income margin in % 16.0 15.6

Revenue Treatments increased by 6 % for the six months ended June 30, 2010 as compared to the same period in 2009 mostly due to same market growth (4 %), contributions from acquisitions (1 %) and the effect of additional treatments related to beginning of the year holiday scheduling in 2010 as compared to the same period in 2009 (1 %). Average North America revenue per treatment was \$ 348 for the six months ended June 30, 2010 and \$ 335 in the same period in 2009. In the U.S., the average revenue per treatment was \$ 356 for the six months ended June 30, 2010 and \$ 341 for the same period in 2009. The increase was mainly attributable to increased commercial payor revenue and overall increased utilization of pharmaceuticals. In addition, there was an increase of 1 % to the 2010 Medicare composite rate.

Net revenue for the North America segment for the first six months of 2010 increased as a result of increases in dialysis care revenue by 10 % to \$ 3,578 million from \$ 3,254 million in the same period of 2009 and in dialysis product revenue by 3 % to \$ 408 million from \$ 396 million in the first six months of 2009.

The dialysis care revenue increase was driven by increased revenue per treatment (4 %), same market treatment growth (4 %) and contributions from acquisitions (2 %), as well as the effect of beginning of the year holiday scheduling in 2010 as compared to the same period in 2009 (1 %), partially offset by the effect of closed or sold clinics (1 %). The administration of EPO represented approximately 20 % of total North America dialysis care revenue for the six-month periods ended June 30, 2010 and 2009.

The dialysis product revenue increase was driven mostly by increased sales of bloodlines, concentrates and dialyzers.

Operating Income Operating income increased to \$ 636 million for the six-month period ended June 30, 2010 from \$ 569 million for the same period in 2009. Operating income margin increased to 16.0 % for the six months ended June 30, 2010 from 15.6 % for the same period in 2009, primarily due to higher revenue per treatment and economies of scale, partially offset by higher personnel expenses and donations to U.S. ESRD patient assistance charities. Cost per treatment increased to \$ 288 for the six-month period ended June 30, 2010 from \$ 283 in the same period of 2009.

International Segment

Key Indicators for International Segment
Table 9
Six months ended June 30, Change
2010 2009 as reported at constant
exchange rates
Number of treatments 5,034,473 4,666,297 8 %
Same market treatment growth in % 4.3 6.6
Revenue in \$ millions 1,842 1,673 10 % 6 %
Depreciation and amortization in \$ millions 98 83 17 %
Operating income in \$ millions 324 300 8 %
Operating income margin in % 17.6 18.0

Revenue Treatments increased by 8 % in the six months ended June 30, 2010 over the same period in 2009 mainly due to same market growth (4 %) and contributions from acquisitions (4 %). Average revenue per treatment for the six months ended June 30, 2010 increased to \$ 162 from \$ 155 in the same period of 2009. An increase of \$ 13 was a result of the strengthening of local currencies against the U.S. dollar while the remaining \$ 3 increase was due to increased reimbursement rates partially offset by growth in countries with lower reimbursement rates.

Net revenues for the International segment for the six-month period ended June 30, 2010 increased by 10 % (6 % increase at constant exchange rates) as compared to the same period in 2009 as a result of increases in both dialysis care and dialysis product revenues. Organic growth during the period was 4 % and acquisitions contributed approximately 2 %, while exchange rate fluctuations accounted for 4 %.

Including the effects of acquisitions, European region revenue increased 7 % (5 % increase at constant exchange rates), Latin America region revenue increased 20 % (9 % increase at constant exchange rates), and Asia Pacific region revenue increased 16 % (7 % increase at constant exchange rates).

Total dialysis care revenue for the International segment increased during the first six months of 2010 by 13 % (9 % increase at constant exchange rates) to \$ 817 million from \$ 723 million in the same period of 2009. This increase is a result of same market treatment growth (4 %), increase in contributions from acquisitions (4 %) and the positive impact increases in revenue per treatment (1 %). Exchange rate fluctuations contributed 4 %.

Total dialysis product revenue for the six-month period ended June 30, 2010 increased by 8 % (4 % increase at constant exchange rates) to \$ 1,025 million from \$ 950 million in the same period of 2009. The increase in product revenue was driven by increased sales of dialyzers, hemodialysis solutions and concentrates as well as bloodlines and products for acute care treatments. Exchange rate fluctuations contributed 4 %.

Operating Income Operating income increased by 8 % to \$ 324 million for the six-month period ended June 30, 2010 from \$ 300 million for the same period in 2009. Operating income margin decreased to 17.6 % for the six-month period ended June 30, 2010 from 18.0 % for the same period in 2009 due to the positive effect of an inventory adjustment in the same period in 2009 and the one-time revaluation of the balance sheet of our operations in Venezuela which was required as a result of the highly inflationary economy of that country and the devaluation of the local currency driven by hyperinflation, partially offset by economies of scale and favorable foreign exchange currency gains.

Inflationary Accounting As we are subject to foreign exchange risk, we monitor the economic conditions of the countries in which we operate. Effective January 1, 2010, our operations in Venezuela are considered to be operating in a highly inflationary economy, as the Venezuelan economy exceeded the three-year cumulative inflation rate of 100 % during the fourth quarter of 2009. We use a blend of the National Consumer Price Index and the Consumer Price Index to determine whether Venezuela is a highly inflationary economy. As a result, our financial statements of our subsidiaries operating in Venezuela have been remeasured as if their functional currency were the U.S. dollar. All gains and losses resulting from the remeasurement of assets and liabilities are reflected in current earnings.

In addition, on January 8, 2010, and effective as of January 11, 2010, the Venezuelan government instituted a two-tier official exchange rate system, resulting in the devaluation of the official rate of the bolivar relative to the U.S. dollar. The rate was previously 2.15 bolivars per \$ 1. A "preferential rate" of 2.6 bolivars per \$ 1 was established for essential items such as medical, food and heavy machinery. All other non-essential items will be imported at the "oil rate" of 4.3 bolivars per \$ 1. Consequently, we recorded a one-time, pre-tax loss of approximately \$ 11.6 million in 2010, primarily reflecting the revaluation of the balance sheet. On a consolidated basis, Venezuela represented less than 1 % of our total revenues in 2009, resulting in a minimal impact on our consolidated results of operations for 2010.

LIQUIDITY AND CAPITAL RESOURCES

Six months ended June 30, 2010 compared to six months ended June 30, 2009.

Liquidity Our primary sources of liquidity have historically been cash from operations, cash from borrowings from third parties and related parties, as well as cash from issuance of equity and debt securities. We require this capital primarily to finance working capital needs, to fund acquisitions and develop free-standing renal dialysis centers, to purchase equipment for existing or new renal dialysis centers and production sites, to repay debt and to pay dividends.

At June 30, 2010, we had cash and cash equivalents of \$ 573 million and short-term bank deposits with an initial term in excess of three months of \$ 123 million. For information regarding utilization and availability under our 2006 Senior Credit Agreement  see Note 6 "Long-term Debt and Capital Lease Obligations" in our Consolidated Financial Statements included in this Report.

Operations In the first six months of 2010 and 2009, we generated cash flows from operations of \$ 643 million and \$ 437 million, respectively. Cash from operations is impacted by the profitability of our business, the development of our working capital, principally receivables, and cash outflows that occur due to a number of singular specific items (especially payments in relation to disallowed tax deductions and legal proceedings). The increase in 2010 versus 2009 was mainly a result of improvements in elements of working capital, decreased levels of inventory and increased earnings, partially offset by higher income tax payments. In addition, there was favorable days sales outstanding (DSO) development in first six months of 2010 as compared to the same period in 2009.

The profitability of our business depends significantly on reimbursement rates. Approximately 75 % of our revenues are generated by providing dialysis treatment, a major portion of which is reimbursed by either public health care organizations or private insurers. For the six-month period ended June 30, 2010, approximately 32 % of our consolidated revenues were attributable to U.S. federal health care benefit programs, such as Medicare and Medicaid reimbursement. Legislative changes could affect Medicare reimbursement rates for all the services we provide, as well as the scope of Medicare coverage. A decrease in reimbursement rates

or the scope of coverage could have a material adverse effect on our business, financial condition and results of operations and thus on our capacity to generate cash flow. In the past we experienced and also expect in the future generally stable reimbursements for our dialysis services. This includes the balancing of unfavorable reimbursement changes in certain countries with favorable changes in other countries.  See "Overview" above for a discussion of recent Medicare reimbursement rate changes including provisions for implementation of a "bundled rate" commencing January 1, 2011.

Our working capital was negative \$ 94 million at June 30, 2010 which decreased from \$ 2,118 million at December 31, 2009, mainly as a result of the reclassification of long-term debt into short-term debt and an increase in accrued expenses and other current liabilities, partially offset by an increase in cash from operations and prepaid expenses and other current assets. Our revolving credit facility and Term Loan A are due on March 31, 2011 and our Trust Preferred Securities are due on June 15, 2011. As a result, these amounts have been reclassified as short-term debt, with \$ 1,386 million related to the revolving credit facility and Term Loan A reclassified during the first quarter of 2010 and \$ 592 million related to the Trust Preferred Securities reclassified during the second quarter of 2010.  See Note 6 "Long-Term Debt and Capital Lease Obligations" in our Consolidated Financial Statements included in this Report for details on the balances outstanding as of June 30, 2010 for the revolving credit facility and Term Loan A. Our ratio of current assets to current liabilities was 1.0 at June 30, 2010.

We will focus our financing activities in the coming years on replacing subordinated debt as necessary with senior notes. We obtained some financing earlier in the current financial year through the issuance of € 250 million principal amount of senior notes, see "Financing" below. Our intention for maturing long-term debt is to extend or renew the 2006 Senior Credit agreement in the latter part of this year as well as to refinance or obtain additional financing for debt maturing in early 2011. On a short-term basis, we have sufficient financial resources, consisting of only partly drawn credit facilities and our accounts receivable facility. We intend, through the extension or renewal of the 2006 Senior Credit Agreement and through obtaining additional financing, to maintain sufficient financial resources in the coming years, with a minimum of \$ 300 to \$ 500 million of committed and unutilized credit facilities.

Cash from operations depends on the collection of accounts receivable. Customers and governments generally have different payment cycles. A lengthening of their payment cycles could have a material adverse effect on our capacity to generate cash flow. In addition, we could face difficulties in enforcing and collecting accounts receivable under some countries' legal systems. Accounts receivable balances at June 30, 2010 and December 31, 2009, net of valuation allowances, represented DSO of approximately 71, respectively.

The development of DSO by operating segment is shown in the table below:

Development of Days Sales Outstanding
Table 10
in days
June 30,
2010
December 31,
2009
North America 51 52
International 113 110
Total 71 72

DSO decreased in the North America segment between December 31, 2009 and June 30, 2010 as a result of continued focus on structural changes within the billing groups, as well as continuing efforts on process improvements to drive cash collections. The increase in DSO for the International segment mainly reflects slight average payment delays by government and private entities most recently impacted by the worldwide financial crises. Due to the fact that a large portion of our reimbursement is provided by public health care organizations and private insurers, we expect that most of our accounts receivables will be collectable, albeit potentially slightly more slowly in the International segment in the immediate future, particularly in countries most severely affected by the global financial crisis. Interest and income tax payments also have a significant impact on our cash from operations.

There are a number of tax and other items we have identified that will or could impact our cash flows from operations in the immediate future as follows:

We filed claims for refunds contesting the Internal Revenue Service's (IRS) disallowance of FMCH's civil settlement payment deductions taken by Fresenius Medical Care Holdings, Inc. (FMCH) in prior year tax returns. As a result of a settlement agreement with the IRS, we received a partial refund in September 2008 of \$ 37 million, inclusive of interest and preserved our right to pursue claims in the United States Courts for refunds of all other disallowed deductions. On December 22, 2008, we filed a complaint for complete refund in the United States District Court for the District of Massachusetts, styled as Fresenius Medical Care Holdings, Inc. v United States. On June 24, 2010, the court denied FMCH's motion for summary judgment and the litigation is proceeding towards trial.

For the tax year 1997, we recognized an impairment of one of our subsidiaries which the German tax authorities disallowed in 2003 at the conclusion of its audit for the years 1996 and 1997. We have filed a complaint with the appropriate German court to challenge the tax authority's decision.

The IRS tax audits of FMCH for the years 2002 through 2006 have been completed. The IRS has disallowed all deductions taken during these audit periods related to intercompany mandatorily redeemable preferred shares. We have protested the disallowed deductions and will avail ourselves of all remedies. An adverse determination with respect to the disallowed deductions related to intercompany mandatorily redeemable preferred shares could have a material adverse effect on our results of operations and liquidity. In addition, the IRS proposed other adjustments which have been recognized in our financial statements.

We are subject to ongoing and future tax audits in the U.S., Germany and other jurisdictions. We have received notices of unfavorable adjustments and disallowances in connection with certain of the audits, including those described above. We are contesting, including appealing, certain of these unfavorable determinations. If our objections and any final audit appeals are unsuccessful, we could be required to make additional tax payments, including payments to state tax authorities reflecting the adjustments made in our federal tax returns in the U.S. With respect to other potential adjustments and disallowances of tax matters currently under review, where tentative agreement has been reached or which are subject to future reviews, we do not anticipate that an unfavorable ruling could have a material impact on our results of operations. We are not currently able to determine the timing of these potential additional tax payments.

W.R. Grace & Co. and certain of its subsidiaries filed for reorganization under Chapter 11 of the U.S. Bankruptcy Code (the Grace Chapter 11 Proceedings) on April 2, 2001. The settlement agreement with the asbestos creditors committees on behalf of the W.R. Grace & Co. bankruptcy estate ( see Note 9 "Commitments and Contingencies – Legal Proceedings – Commercial Litigation") provides for payment by the Company of \$ 115 million upon approval of the settlement agreement by the U.S. District Court, which has occurred, and confirmation of a W.R. Grace & Co. bankruptcy reorganization plan that includes the settlement. The \$ 115 million

obligation was included in the special charge we recorded in 2001 to address 1996 merger-related legal matters. The payment obligation is not interest-bearing.

If all potential additional tax payments and the Grace Chapter 11 Proceedings settlement payment were to occur contemporaneously, there could be a material adverse impact on our operating cash flow in the relevant reporting period. Nonetheless, we anticipate that cash from operations and, if required, our senior credit agreement and other sources of liquidity will be sufficient to satisfy all such obligations if and when they come due.

Investing We used net cash of \$ 501 million and \$ 280 million in investing activities in the six-month periods ended June 30, 2010 and 2009, respectively.

Capital expenditures for property, plant and equipment, net of disposals were \$ 218 million in the first six months of 2010 and \$ 249 million in the same period in 2009. In the first six months of 2010, capital expenditures were \$ 129 million in the North America segment and \$ 89 million for the International segment. Capital expenditures in the first six months of 2009 were \$ 147 million in the North America segment and \$ 102 million for the International segment. The majority of our capital expenditures was used for maintaining existing clinics, equipping new clinics, and maintenance and expansion of production facilities primarily in North America and Germany and capitalization of machines provided to our customers, primarily in the International segment. Capital expenditures were approximately 4 % and 5 % of total revenue in the first six months of 2010 and 2009, respectively.

We invested approximately \$ 158 million cash in the first six months of 2010, primarily for acquisitions of dialysis clinics (\$ 50 million in the North America segment, \$ 102 million in the International segment and \$ 6 million at Corporate), as compared to \$ 82 million cash in the same period of 2009 (\$ 36 million in the North America segment and \$ 46 million in the International segment). In addition, we invested \$ 133 million (€ 100 million) in short-term investments with banks during the first six months of 2010. We also received \$ 8 million and \$ 51 million in conjunction with divestitures in the first six months of 2010 and 2009, respectively.

We anticipate capital expenditures of approximately \$ 550 to \$ 650 million and expect to make acquisitions of up to \$ 500 million in 2010. See "Outlook" below.

Financing Net cash provided by financing was \$ 170 million in the first six months of 2010 compared to net cash used in financing of \$ 155 million in the first six months of 2009.

In the first six months of 2010, cash was mainly provided by borrowings under the revolving credit facility, our issuance of 5.5 % Senior Notes in January 2010 and drawings under the accounts receivable facility. Part of these funds was used to pay dividends. In the first six months of 2009, cash was mainly used for the payment of dividends.

On May 11, 2010, we paid a dividend with respect to 2009 of € 0.61 per ordinary share (for 2008 paid in 2009: € 0.58) and € 0.63 per preference share (for 2008 paid in 2009: € 0.60). The total dividend payment was € 183 million (\$ 232 million) compared to € 173 million (\$ 232 million) in 2009 with respect to 2008.

On February 17, 2010, a € 50 million (\$ 61.4 million at June 30, 2010) loan was disbursed from our 2009 agreement with the European Investment Bank (EIB). The loan is due in 2014. In addition, on March 15, 2010, we drew down the remaining \$ 80.8 million available on our 2005 revolving credit agreement with the EIB, maturing in 2013. Both loans bear variable interest rates which are based on EURIBOR or LIBOR, as applicable, plus an applicable margin. These interest rates change every three months.

On January 20, 2010, our wholly owned subsidiary, FMC Finance VI S.A., issued € 250 million (\$ 353.3 million at date of issuance) aggregate principal amount of 5.50 % Senior Notes at an issue price of 98.6636 % of the principal amount. The 5.50 % Senior Notes had a yield to maturity of 5.75 % and are due July 15, 2016. Proceeds were used to repay short-term indebtedness and for general corporate purposes. The 5.50 % Senior Notes are guaranteed on a senior basis jointly and severally by us, Fresenius Medical Care Holdings, Inc. and Fresenius Medical Care Deutschland GmbH.

The rating agencies identified in the table below assign credit ratings to us based on their assessments of our financing strategy, resources and financial performance. Our cost of borrowing is indirectly influenced by these ratings. The table below shows the ratings and outlook as of August 3, 2010:

ratings
Table 11
Standard & Poor´s Moody´s Fitch
Corporate Credit Rating BB Ba1 BB
Outlook positive stable positive

Debt covenant disclosure – EBITDA EBITDA (earnings before interest, tax, depreciation and amortization expenses) was approximately \$ 1,134 million, 19.4 % of revenues for the six-month period ended June 30, 2010, and \$ 1.029 million, 19.3 % of revenues for the same period of 2009. EBITDA is the basis for determining compliance with certain covenants contained in our 2006 Senior Credit Agreement, Euro Notes, EIB, and the indentures relating to our 6 7/8 % Senior Notes, our 5.50 % Senior Notes and our outstanding trust preferred securities. You should not consider EBITDA to be an alternative to net earnings determined in accordance with U.S. GAAP or to cash flow from operations, investing activities or financing activities. In addition, not all funds depicted by EBITDA are available for management's discretionary use. For example, a substantial portion of such funds are subject to contractual restrictions and functional requirements for debt service, to fund necessary capital expenditures and to meet other commitments from time to time as described in more detail elsewhere in this report. EBITDA, as calculated, may not be comparable to similarly titled measures reported by other companies. A reconciliation of EBITDA to cash flow provided by operating activities, which we believe to be the most directly comparable U.S. GAAP financial measure, is calculated as follows:

Reconciliation of measures for consolidated totals
Table 12
in \$ thousands
Six months ended June 30,
2010 2009
Total EBITDA 1,133,532 1,029,321
Interest expense (net of interest income) (135,649) (149,524)
Income tax expense, net (256,603) (213,749)
Change in deferred taxes, net 747 29,281
Changes in operating assets and liabilities (108,844) (273,002)
Stock compensation expense 13,712 14,991
Other items, net (1,938) (1)
Net cash provided by operating activities 643,463 437,317

Balance Sheet Structure Total assets as of June 30, 2010 increased to \$ 16.0 billion compared to \$ 15.8 billion at year-end 2009. Current assets as a percent of total assets increased slightly to 31 % at June 30, 2010 from 30 % at December 31, 2009. The equity ratio, the ratio of our equity divided by total liabilities and shareholders' equity, decreased to 43 % at June 30, 2010 from 44 % at year-end 2009.

Outlook We have increased our estimated expenditures for acquisitions in 2010 from up to \$ 400 million to up to \$ 500 million and otherwise confirmed our outlook for the full year 2010 as depicted in the table below:

in \$  millions, except
Debt/EBITDA ratio
outlook
Table 13
2010
Net revenue >12,000
Net income attributable to FMC-AG & Co. KGaA 950 – 980
Debt/ EBITDA < 2.5
Capital Expenditures ~ 550 – 650
Acquisitions up to 500

Recently Issued Accounting Standards In July 2010, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update 2010-20 (ASU 2010-20), Disclosures about the Credit Quality of Financing Receivables and the Allowance for Credit Losses. ASU 2010-20 is an update of Accounting Standards Codification Topic 310, Receivables. This update requires enhanced disclosures on a disaggregated basis about:

  • The nature of the credit risk inherent in the portfolio of financing receivables
  • How that risk is analyzed and assessed in arriving at the allowance for credit losses
  • The changes and reasons for those changes in the allowance for credit losses.

The disclosures required under ASU 2010-20 as of the end of a reporting period are effective for interim and annual reporting periods ending on or after December 15, 2010. Disclosures about activity that occurs during a reporting period are effective for interim and annual reporting periods beginning on or after December 15, 2010. We are currently evaluating the impact of ASU 2010-20 on our consolidated financial statements.

Consolidated Financial Statements 26

Consolidated Statements of Income

consolidated statements of income
in \$ thousands, except per Table 14
share data, unaudited
Three months ended June 30, Six months ended June 30,
2010 2009 2010 2009
Net revenue
Dialysis care 2,224,321 2,054,104 4,395,105 3,977,425
Dialysis products 721,878 709,465 1,433,223 1,345,954
total 2,946,199 2,763,569 5,828,328 5,323,379
Costs of revenue
Dialysis care 1,554,649 1,474,043 3,096,330 2,870,850
Dialysis products 379,942 357,814 756,098 658,512
total 1,934,591 1,831,857 3,852,428 3,529,362
Gross profit 1,011,608 931,712 1,975,900 1,794,017
Operating expenses
Selling, general and administrative 525,557 495,119 1,043,271 938,686
Research and development 21,373 18,956 44,462 41,852
Operating income 464,678 417,637 888,167 813,479
Other (income) expense
Interest income (8,244) (7,899) (14,083) (12,173)
Interest expense 76,468 83,133 149,732 161,697
Income before income taxes 396,454 342,403 752,518 663,955
Income tax expense 129,075 103,369 256,603 213,749
Net income 267,379 239,034 495,915 450,206
Less: Net income attributable to noncontrolling interests 19,110 17,921 36,530 30,987
Net income attributable to FMC-AG
& Co. KG
AA
248,269 221,113 459,385 419,219
Basic income per ordinary share 0.83 0.74 1.53 1.41
Fully diluted income per ordinary share 0.82 0.74 1.52 1.41

Consolidated Statements of comprehensive Income

Consolidated Statements of Comprehensive Income
in \$ thousands,
unaudited
Table 15
Three months ended June 30, Six months ended June 30,
2010 2009 2010 2009
Net Income 267,379 239,034 495,915 450,206
(Loss) gain related to cash flow hedges (55,489) 15,785 (72,951) 15,846
Actuarial gains on defined benefit pension plans 1,220 1,218 2,410 2,436
Forreign currency translation (184,969) 113,274 (309,906) 28,261
Income tax benefit (expense) related to components of other
comprehensive income
14,271 (7,636) 19,152 (8,718)
Other comprehensive (loss) income, net of tax (224,967) 122,641 (361,295) 37,825
Total comprehensive income 42,412 361,675 134,620 488,031
Comprehensive income attributable to noncontrolling interests 19,325 19,807 35,630 31,894
Comprehensive income attributable to
FMC-AG
& Co. KG
aA
23,087 341,868 98,990 456,137

Consolidated Balance Sheets

consolidated balance sheets
Table 16
in \$ thousands, except
share data
June 30, December 31,
(unaudited) (audited)
2010 2009
Assets
Current assets
Cash and cash equivalents 572,851 301,225
Trade accounts receivable less allowance for doubtful accounts of \$272,872 in 2010 and \$ 266,449 in 2009 2,259,355 2,285,909
Accounts receivable from related parties 109,799 272,886
Inventories 810,016 821,654
Prepaid expenses and other current assets 888,388 729,306
Deferred taxes 311,434 316,820
Total current assets 4,951,843 4,727,800
Property, plant and equipment, net 2,332,580 2,419,570
Intangible assets 635,078 859,195
Goodwill 7,734,442 7,511,434
Deferred taxes 84,305 64,749
Other assets 261,316 238,567
Total assets 15,999,564 15,821,315
Liabilities and shareholders' equity
Current liabilities
Accounts payable 362,512 362,407
Accounts payable to related parties 113,351 277,429
Accrued expenses and other current liabilities 1,592,630 1,335,553
Short-term borrowings and other financial liabilities 410,057 316,344
Short-term borrowings from related parties 8,893 10,440
Current portion of long-term debt and capital lease obligations 1,866,410 157,634
Company-obligated mandatorily redeemable preferred securities of subsidiary Fresenius Medical Care Capital Trusts
holding solely company-guaranteed debentures of subsidiaries, current portion 592,478
Income tax payable 75,787 116,978
Deferred taxes 24,100 32,930
Total current liabilities 5,046,218 2,609,715
Long-term debt and capital lease obligations, less current portion 2,948,899 4,427,921
Other liabilities 288,210 307,112
Pension liabilities 135,090 147,327
Income tax payable 215,867 215,921
Deferred taxes 435,827 427,530
Company-obligated mandatorily redeemable preferred securities of subsidiary Fresenius Medical Care Capital Trusts
holding solely company-guaranteed debentures of subsidiaries 656,096
Total liabilities 9,070,111 8,791,622
Shareholders´ equity
Preference shares, no par value, €1.00 nominal value, 12,356,880 shares authorized, 3,908,683 issued and outstanding 4,375 4,343
Ordinary shares, no par value, €1.00 nominal value, 373,436,220 shares authorized, 296,478,496 issued and outstanding 366,656 365,672
Additional paid-in capital 3,427,806 3,389,111
Retained earnings 3,338,948 3,111,530
Accumulated other comprehensive (loss) income (410,119) (49,724)
Total FMC-AG & Co. KGAA shareholders' equity 6,727,666 6,820,932
Noncontrolling interests 201,787 208,761
Total equity 6,929,453 7,029,693
Total liabilities and equity 15,999,564 15,821,315

Consolidated statements of cash flows

Consolidated Statements of Cash Flows
Table 17
in \$ thousands,
unaudited
Six months ended June 30,
2010 2009
Operating Activities
Net income 495,915 450,206
Adjustments to reconcile net income to net cash provided by operating activities:
Depreciation and amortization 245,365 215,842
Change in deferred taxes, net (747) 29,281
(Gain) on sale of investments (1,852) (652)
(Gain) loss on sale of fixed assets (86) 651
Compensation expense related to stock options 13,712 14,991
Changes in assets and liabilities, net of amounts from businesses acquired:
Trade accounts receivable, net (94,298) (59,116)
Inventories (33,482) (129,724)
Prepaid expenses, other current and non-current assets (87,687) (102,714)
Accounts receivable from related parties 128,263 (3,361)
Accounts payable to related parties (133,600) 301
Accounts payable, accrued expenses and other current and non-current liabilities 129,381 36,358
Income tax payable (17,421) (14,746)
Net cash provided by operating activities 643,463 437,317
Investing Activities
Purchases of property, plant and equipment (226,635) (253,865)
Proceeds from sale of property, plant and equipment 8,582 4,321
Acquisitions and investments, net of cash acquired, and net purchases of intangible assets (291,247) (81,483)
Proceeds from divestitures 7,867 50,918
Net cash ( used in ) investing activities (501,433) (280,109)
Financing Activities
Proceeds from short-term borrowings and other financial liabilities 1,052,674 40,518
Repayments of short-term borrowings and other financial liabilities (1,045,870) (95,179)
Proceeds from short-term borrowings from related parties 15,994
Repayments of short-term borrowings from related parties (17,251)
Proceeds from long-term debt and capital lease obligations
(net of debt issuance costs of \$10,218 in 2010) 828,735 589,613
Repayments of long-term debt and capital lease obligations (495,003) (258,034)
Increase (decrease) of accounts receivable securitization program 86,000 (190,000)
Proceeds from exercise of stock options 28,084 12,745
Dividends paid (231,967) (231,940)
Distributions to noncontrolling interests (67,562) (28,174)
Contributions from noncontrolling interests 14,850 7,013
Net cash provided by ( used in ) financing activities 169,941 (154,695)
Eff
ect of exchange rate changes on cash and cash equivalents
(40,345) 5,554
Cash and Cash Equivalents
Net increase in cash and cash equivalents 271,626 8,067
Cash and cash equivalents at beginning of period 301,225 221,584
Cash and cash equivalents at end of period 572,851 229,651

Consolidated statements of shareholders´ equity

consolidated statements of shareholders' equity
in \$ thousands, except share
and per share data, unaudited
Table 18
Preference Shares Ordinary Shares
Number of
shares
No par value
in \$
Number of
shares
No par value
in \$
Balance at December 31, 2008 3,810,540 4,240 293,932,036 363,076
Proceeds from exercise of options and related tax effects 73,788 103 1,814,599 2,596
Compensation expense related to stock options
Dividends paid
Purchase / sale of noncontrolling interests
Contributions from noncontrolling interests
Net income
Other comprehensive income (loss)
Comprehensive income
Balance at December 31, 2009 3,884,328 4,343 295,746,635 365,672
Proceeds from exercise of options and related tax effects 24,355 32 731,861 984
Compensation expense related to stock options
Dividends paid
Purchase / sale of noncontrolling interests
Contributions from noncontrolling interests
Net income
Other comprehensive income (loss)
Comprehensive (loss) income
Balance at June 30, 2010 3,908,683 4,375 296,478,496 366,656
consolidated statements of shareholders' equity
in \$ thousands, except share Table 18
and per share data, unaudited
Additional
paid in
capital
Retained
earnings
Accumulated
Other
comprehen
sive income
(loss )
Total
FMC-AG&
Co.KGaA
shareholders´
equity
Non
controlling
interests
Total
Balance at December 31, 2008 3,293,918 2,452,332 (151,284) 5,962,282 160,504 6,122,786
Proceeds from exercise of options and
related tax effects
64,585 67,284 67,284
Compensation expense related to stock options 33,746 33,746 33,746
Dividends paid (231,940) (231,940) (61,499) (293,439)
Purchase /sale of noncontrolling interests (3,138) (3,138) 25,477 22,339
Contributions from noncontrolling interests 8,393 8,393
Net income 891,138 891,138 74,082 965,220
Other comprehensive income (loss) 101,560 101,560 1,804 103,364
Comprehensive income 992,698 75,886 1,068,584
Balance at December 31, 2009 3,389,111 3,111,530 (49,724) 6,820,932 208,761 7,029,693
Proceeds from exercise of options and
related tax effects
25,850 26,866 26,866
Compensation expense related to stock options 13,712 13,712 13,712
Dividends paid (231,967) (231,967) (58,740) (290,707)
Purchase /sale of noncontrolling interests (867) (867) 10,123 9,256
Contributions from noncontrolling interests 6,013 6,013
Net income 459,385 459,385 36,530 495,915
Other comprehensive income (loss) (360,395) (360,395) (900) (361,295)
Comprehensive (loss) income 98,990 35,630 134,620
Balance at June 30, 2010 3,427,806 3,338,948 (410,119) 6,727,666 201,787 6,929,453

Notes to Consolidated Financial Statements

Unaudited. In thousands, except share and per share data.

1. The Company, Basis of Presentation, Significant accounting policies and health care reform The Company Fresenius Medical Care AG & Co. KGaA (FMC-AG & Co. KGaA or the Company), a German partnership limited by shares (Kommanditgesellschaft auf Aktien), is the world's largest kidney dialysis company, operating in both the field of dialysis services and the field of dialysis products for the treatment of end-stage renal disease (ESRD). The Company's dialysis business is vertically integrated, providing dialysis treatment at dialysis clinics it owns or operates and supplying these clinics with a broad range of products. In addition, the Company sells dialysis products to other dialysis service providers. In the United States, the Company also performs clinical laboratory testing and provides inpatient dialysis services and other services under contract to hospitals. In this report, "FMC-AG & Co. KGaA" or the "Company", "we", "us" or "our" refers to the Company or the Company and its subsidiaries on a consolidated basis, as the context requires.

Basis of Presentation The accompanying consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America (U.S. GAAP).

The consolidated financial statements at June 30, 2010 and for the three- and six-month periods ended June 30, 2010 and 2009 contained in this report are unaudited and should be read in conjunction with the consolidated financial statements contained in the Company's 2009 Annual Report on Form 20-F. The preparation of consolidated financial statements requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the consolidated financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates. Such financial statements reflect all adjustments that, in the opinion of management, are necessary for a fair presentation of the results of the periods presented. All such adjustments are of a normal recurring nature.

The results of operations for the three- and six-month periods ended June 30, 2010 are not necessarily indicative of the results of operations for the year ending December 31, 2010.

Summary of significant accounting policies - Cash equivalents and short-term investments Cash equivalents include highly liquid short-term investments with original maturities of three months or less, readily convertible into known amounts of cash. Investments with original maturities greater than three months and remaining maturities of less than one year are classified as short-term investments. Short-term investments classified as available-for-sale are recorded at fair value with unrealized gains or losses reflected in accumulated other comprehensive income until realized. Short-term investments designated as held-tomaturity securities are recorded at amortized cost. These investments are included in prepaid expenses and other current assets on the balance sheet.

At June 30, 2010, the Company had \$ 122,710 (€ 100,000) of held-to-maturity, short-term investments. These investments are valued at their carrying amounts, which are reasonable estimates of the fair value due to the relatively short period to maturity of these investments.

United States health care reform The Patient Protection and Affordable Care Act was enacted in the United States on March 23, 2010 and subsequently amended by the Health Care and Educational Affordability Reconciliation Act (as amended, PPACA). PPACA will implement broad healthcare system reforms, including (i) provisions to facilitate access to affordable health insurance for all Americans, (ii) expansion of the Medicaid program, (iii) an industry fee on pharmaceutical companies starting in 2011 based on sales of brand name pharmaceuticals to government healthcare programs, (iv) a 2.3 % excise tax on manufacturers' medical device sales starting in 2013, (v) increases in Medicaid prescription drug rebates effective January 1, 2010, (vi) commercial insurance market reforms that protect consumers, such as bans on lifetime and annual limits, coverage of pre-existing conditions, and limits on waiting periods, (vii) provisions encouraging integrated care, efficiency and coordination among providers and (viii) provisions for reduction of healthcare program waste and fraud. PPACA does not modify the dialysis reimbursement provisions of the Medicare Improvements for Patients and Providers Act of 2008. PPACA's medical device excise tax, Medicaid drug rebate increases and annual pharmaceutical industry fees will adversely impact the Company's product business earnings and cash flows. The Company expects modest favorable impact from PPACA's integrated care and commercial insurance consumer protection provisions.

2. Related Party Transactions

a ) Service and Lease Agreements The Company is party to service agreements with Fresenius SE, the sole stockholder of its General Partner and its largest shareholder owning approximately 36.0 % of the Company's voting shares, and with certain affiliates of Fresenius SE that are not also subsidiaries of the Company (collectively Fresenius SE), to receive services, including, but not limited to: administrative services, management information services, employee benefit administration, insurance, IT services, tax services and treasury management services. For the six-month periods ended June 30, 2010 and 2009, amounts charged by Fresenius SE to the Company under the terms of these agreements are \$ 32,099 and \$ 32,139, respectively. The Company also provides certain services to Fresenius SE, including research and development, central purchasing, patent administration and warehousing. The Company charged \$ 3,269 and \$ 9,206 for services rendered to Fresenius SE during the first six months of 2010 and 2009, respectively.

Under operating lease agreements for real estate entered into with Fresenius SE, the Company paid Fresenius SE \$ 9,689 and \$ 9,766 during the first six months of 2010 and 2009, respectively. The majority of the leases expire in 2016 and contain renewal options.

The Company's Articles of Association provide that the General Partner shall be reimbursed for any and all expenses in connection with management of the Company's business, including remuneration of the members of the General Partner's supervisory board and the General Partner's management board. The aggregate amount reimbursed to the General Partner for the six-month periods ended June 30, 2010 and 2009 was \$ 4,983 and \$ 3,619, respectively, for its management services during those six-month periods.

b ) Products For the six-month periods ended June 30, 2010, and 2009, the Company sold products to Fresenius SE for \$ 7,184 and \$ 7,332, respectively. During the six-month periods ended June 30, 2010, and 2009, the Company made purchases from Fresenius SE in the amount of \$ 22,553 and \$ 22,303, respectively.

In addition to the purchases noted above, the Company currently purchases heparin supplied by APP Inc., through a group purchasing organization (GPO). In September 2008, Fresenius Kabi AG, a wholly-owned subsidiary of Fresenius SE, acquired 100 % of APP Inc. The Company has no direct supply agreement with APP Inc. and does not submit purchase orders directly to APP Inc. During the six-month periods ended June 30, 2010 and 2009, Fresenius Medical Care Holdings, Inc. (FMCH) acquired approximately \$ 15,591 and \$ 17,421, respectively, of heparin from APP Inc. through the GPO contract, which was negotiated by the GPO at arm's length on behalf of all members of the GPO.

c ) Financing Provided by and to Fresenius SE Throughout the second quarter of 2010, the Company, under its cash pooling agreement, made cash advancements to Fresenius SE totaling € 161,800 (\$ 198,545 as of June 30, 2010), at an interest rate of 1.02 %. The total amount was due on July 31, 2010. The remaining balance of \$ 143,178 (€ 109,900) on July 31, 2010 was extended until August 31, 2010 at an interest rate of 1.09 %. On June 30, 2009, under the cash pooling agreement, the Company made a cash advancement of \$ 25,159 to Fresenius SE at 1.16 % interest which was repaid on July 6, 2009.

During the second quarter of 2009, the Company reclassified an account payable to Fresenius SE in the amount of € 77,745 (\$ 109,885 at June 30, 2009) from accounts payable to related parties to short-term borrowings from related parties. The amount represents taxes payable by the Company arising from the period 1997-2001 during which German trade taxes were paid by Fresenius SE on behalf of the Company. Of this amount, € 5,747 (\$ 7,052 at June 30, 2010) was outstanding at June 30, 2010 at an interest rate of 6 % and will be repaid in 2010.

On August 19, 2009, the Company borrowed € 1,500 (\$ 1,841 as of June 30, 2010) from the General Partner at 1.335 %, due on August 19, 2010.

On November 7, 2008, the Company entered into a loan agreement with Fresenius SE whereby it advanced Fresenius SE \$ 50,000 at 6.45 % interest which was due and repaid on April 30, 2009.

Inventories
Table 19
in \$ thousands
June 30,
2010
December 31,
2009
Raw materials and purchased components 143,424 154,599
Work in process 63,516 63,683
Finished goods 491,483 481,047
Health care supplies 111,593 122,325
inventories 810,016 821,654

3. Inventories As of June 30, 2010 and December 31, 2009, inventories consisted of the following:

4. Intangible Assets and Goodwill On April 1, 2010 the Company received approval from the state of New York to directly own facilities in that state. This direct ownership had previously been prohibited by state law. Due to this prohibition, the Company had historically used a combination of administrative service contracts, stock option agreements, and asset acquisitions to qualify for consolidation of such facilities under guidance originally issued as Emerging Issues Task Force 97-2, Application of FASB Statement No. 94 and APB Opinion No. 16 to Physicians Practice Management Entities and Certain Other Entities with Contractual Management Arrangements which is now included within FASB Accounting Standards Codification Topic 810-10, Consolidation: Overall. In such qualifying transactions, a portion of the purchase price was allocated to identifiable intangible assets with the remainder classified as an "Administrative Services Agreement" intangible asset that was treated as an equivalent to goodwill and was shown on our Balance Sheet at December 31, 2009, under the category Management Contracts within Intangible Assets. With the regulatory approval, the Company obtained the full ownership of these facilities and reclassified the \$ 214,706 (€ 161,786) of Administrative Services Agreement intangible asset to goodwill within our North America segment, effective April 1, 2010, to be consistent with other clinic acquisitions where the Company obtained control via legal ownership.

5. Short-Term Borrowings, Other Financial Liabilities and Short-Term Borrowings from Related

Parties As of June 30, 2010 and December 31, 2009, short-term borrowings, other financial liabilities and short-term borrowings from related parties consisted of the following:

Short-term borrowings
Table 20
in \$ thousands
June 30,
2010
December 31,
2009
Borrowings under lines of credit 101,373 95,720
Accounts receivable facility 300,000 214,000
Other financial liabilities 8,684 6,624
Short-term borrowings and other financial liabilities 410,057 316,344
Short-term borrowings from related parties  see Note 2c 8,893 10,440
Short-term borrowings, other financial liabilities and short-term
borrowing from related parties
418,950 326,784

6. Long-term Debt and Capital Lease Obligations As of June 30, 2010 and December 31, 2009, long-term debt and capital lease obligations consisted of the following:

Long-term debt and Capital Lease Obligations
Table 21
in \$ thousands
June 30,
2010
December 31,
2009
2006 Senior Credit Agreement 3,375,326 3,522,040
6 7/8 % Senior Notes 493,788 493,344
5.50 % Senior Notes 302,938
Euro Notes 245,420 288,120
EIB Agreements 336,412 213,460
Capital lease obligations 15,461 17,600
Other 45,964 50,991
4,815,309 4,585,555
Less current maturities (1,866,410) (157,634)
total 2,948,899 4,427,921

available and outstanding credits Table 22 Maximum Amount Available June 30, December 31, 2010 2009 Balance Outstanding June 30, December 31, 2010 2009 Revolving Credit 1,000,000 1,000,000 514,933 594,714 Term Loan A 1,314,557 1,373,418 1,314,557 1,373,418 Term Loan B 1,545,836 1,553,908 1,545,836 1,553,908 total 3,860,393 3,927,326 3,375,326 3,522,040 in \$ thousands

2006 Senior Credit Agreement The following table shows the available and outstanding amounts under the 2006 Senior Credit Agreement at June 30, 2010 and December 31, 2009:

In addition, at June 30, 2010 and December 31, 2009, the Company had letters of credit outstanding in the amount of \$ 121,518 and \$ 97,287, respectively, which are not included above as part of the balance outstanding at those dates but which reduce available borrowings under the revolving credit facility.

7. Earnings Per Share The following table contains reconciliations of the numerators and denominators of the basic and diluted earnings per share computations for the three- and six-month periods ended June 30, 2010 and 2009:

Reconciliation of Basic and Diluted Earnings per Share
in \$ thousands, except
per share data
Table 23
Three months ended June 30, Six months ended June 30,
2010 2009 2010 2009
Numerators
Net income attributable to FMC-AG&Co. KGaA 248,269 221,113 459,385 419,219
Less dividend preference on Preference shares 25 26 51 50
Income available to all classes of shares 248,244 221,087 459,334 419,169
Denominators
Weighted average number of:
Ordinary shares outstanding 296,104,554 294,163,999 295,926,583 294,048,658
Preference shares outstanding 3,899,075 3,827,962 3,894,560 3,819,676
Total weighted average shares outstanding 300,003,629 297,991,961 299,821,143 297,868,334
Potentially dilutive Ordinary shares 1,775,499 1,594,139 71,033
Potentially dilutive Preference shares 49,206 65,260 46,919 70,715
Total weighted average Ordinary shares outstanding
assuming dilution
297,880,053 294,163,999 297,520,722 294,119,691
Total weighted average Preference shares outstanding
assuming dilution
3,948,281 3,893,222 3,941,479 3,890,391
Basic income per Ordinary share 0.83 0.74 1.53 1.41
Plus preference per Preference shares 0.01 0.02 0.01
Basic income per Preference share 0.83 0.75 1.55 1.42
Fully diluted income per Ordinary share 0.82 0.74 1.52 1.41
Plus preference per Preference shares 0.01 0.01 0.02 0.01
Fully diluted income per Preference share 0.83 0.75 1.54 1.42

8. Employee Benefit Plans The Company currently has two principal pension plans, one for German employees, the other covering employees in the United States, the latter of which was curtailed in 2002. Plan benefits are generally based on years of service and final salary. Consistent with predominant practice in Germany, the Company's pension obligations in Germany are unfunded. Each year FMCH, a wholly-owned subsidiary of the Company and its principal North American subsidiary, contributes to the plan covering United States employees at least the minimum required by the Employee Retirement Income Security Act of 1974, as amended.

The following table provides the calculations of net periodic benefit cost for the three- and six-month periods ended June 30, 2010 and 2009.

in \$ thousands Employee benefit plans
Table 24
Three months ended June 30, Six months ended June 30,
2010 2009 2010 2009
Components of net periodic benefit cost
Service cost 1,915 1,966 3,965 3,868
Interest cost 5,521 5,359 11,188 10,644
Expected return on plan assets (4,366) (3,965) (8,732) (7,930)
Amortization of unrealized losses 1,221 1,218 2,411 2,436
Net periodic benefit costs 4,291 4,578 8,832 9,018

9. Commitments and Contingencies

Legal Proceedings The Company is routinely involved in numerous claims, lawsuits, regulatory and tax audits, investigations and other legal matters arising, for the most part, in the ordinary course of its business of providing healthcare services and products. The outcome of litigation and other legal matters is always difficult to accurately predict and outcomes that are not consistent with the Company's view of the merits can occur. The Company believes that it has valid defenses to the legal matters pending against it and is defending itself vigorously. Nevertheless, it is possible that the resolution of one or more of the legal matters currently pending or threatened could have a material adverse effect on its business, results of operations and financial condition.

Commercial Litigation The Company was originally formed as a result of a series of transactions it completed pursuant to the Agreement and Plan of Reorganization dated as of February 4, 1996, by and between W.R. Grace & Co. and Fresenius SE (the Merger). At the time of the Merger, a W.R. Grace & Co. subsidiary known as W.R. Grace & Co.-Conn. had, and continues to have, significant liabilities arising out of productliability related litigation (including asbestos-related actions), pre-Merger tax claims and other claims unrelated to National Medical Care, Inc. (NMC), which was W.R. Grace & Co.'s dialysis business prior to the Merger. In connection with the Merger, W.R. Grace & Co.-Conn. agreed to indemnify the Company, FMCH, and NMC against all liabilities of W.R. Grace & Co., whether relating to events occurring before or after the Merger, other than liabilities arising from or relating to NMC's operations. W.R. Grace & Co. and certain of its subsidiaries filed for reorganization under Chapter 11 of the U.S. Bankruptcy Code (the Grace Chapter 11 Proceedings) on April 2, 2001.

Prior to and after the commencement of the Grace Chapter 11 Proceedings, class action complaints were filed against W.R. Grace & Co. and FMCH by plaintiffs claiming to be creditors of W.R. Grace & Co.-Conn., and by the asbestos creditors' committees on behalf of the W.R. Grace & Co. bankruptcy estate in the Grace Chapter 11 Proceedings, alleging among other things that the Merger was a fraudulent conveyance, violated the uniform fraudulent transfer act and constituted a conspiracy. All such cases have been stayed and transferred to or are pending before the U.S. District Court as part of the Grace Chapter 11 Proceedings.

In 2003, the Company reached agreement with the asbestos creditors' committees on behalf of the W.R. Grace & Co. bankruptcy estate and W.R. Grace & Co. in the matters pending in the Grace Chapter 11 Proceedings for the settlement of all fraudulent conveyance and tax claims against it and other claims related to the Company that arise out of the bankruptcy of W.R. Grace & Co. Under the terms of the settlement agreement as amended (the Settlement Agreement), fraudulent conveyance and other claims raised on behalf of asbestos claimants will be dismissed with prejudice and the Company will receive protection against existing and potential future W.R. Grace & Co. related claims, including fraudulent conveyance and asbestos claims, and indemnification against income tax claims related to the non-NMC members of the W.R. Grace & Co. consolidated tax group upon confirmation of a W.R. Grace & Co. bankruptcy reorganization plan that contains such provisions. Under the Settlement Agreement, the Company will pay a total of \$ 115,000 without interest to the W.R. Grace & Co. bankruptcy estate, or as otherwise directed by the Court, upon plan confirmation. No admission of liability has been or will be made. The Settlement Agreement has been approved by the U.S. District Court. Subsequent to the Merger, W.R. Grace & Co. was involved in a multi-step transaction involving Sealed Air Corporation (Sealed Air, formerly known as Grace Holding, Inc.). The Company is engaged in litigation with Sealed Air to confirm its entitlement to indemnification from Sealed Air for all losses and expenses incurred by the Company relating to pre-Merger tax liabilities and Merger-related claims. Under the Settlement Agreement, upon confirmation of a plan that satisfies the conditions of the Company's payment obligation, this litigation will be dismissed with prejudice.

On April 4, 2003, FMCH filed a suit in the U.S. District Court for the Northern District of California, styled Fresenius USA, Inc., et al., v. Baxter International Inc., et al., Case No. C 03-1431, seeking a declaratory judgment that FMCH does not infringe patents held by Baxter International Inc. and its subsidiaries and affiliates (Baxter), that the patents are invalid, and that Baxter is without right or authority to threaten or maintain suit against FMCH for alleged infringement of Baxter's patents. In general, the alleged patents concern the use of touch screen interfaces for hemodialysis machines. Baxter filed counterclaims against FMCH seeking more than \$ 140,000 in monetary damages and injunctive relief, and alleging that FMCH willfully infringed on Baxter's patents. On July 17, 2006, the court entered judgment on a jury verdict in favor of FMCH finding that all the asserted claims of the Baxter patents are invalid as obvious and/or anticipated in light of prior art.

On February 13, 2007, the court granted Baxter's motion to set aside the jury's verdict in favor of FMCH and reinstated the patents and entered judgment of infringement. Following a trial on damages, the court entered judgment on November 6, 2007 in favor of Baxter on a jury award of \$ 14,300. On April 4, 2008, the court denied Baxter's motion for a new trial, established a royalty payable to Baxter of 10 % of the sales price for continuing sales of FMCH's 2008K hemodialysis machines and 7 % of the sales price of related disposables, parts and service beginning November 7, 2007, and enjoined sales of the touchscreen-equipped 2008K machine effective January 1, 2009. The Company appealed the court's rulings to the Court of Appeals for the Federal Circuit. In October 2008, the Company completed design modifications to the 2008K machine that eliminate any incremental hemodialysis machine royalty payment exposure under the original district court order. On September 10, 2009, the Court of Appeals reversed the district court's decision and determined that the asserted claims in two of the three patents at issue are invalid. As to the third patent, the Court of Appeals affirmed the district court's decision; however, the Court of Appeals vacated the injunction and award of damages. These issues were remanded to the District Court for reconsideration in light of the invalidity ruling

on most of the claims. As a result, FMCH is no longer required to fund the court-approved escrow account set up to hold the royalty payments ordered by the district court, although funds already contributed will remain in escrow until the case is finally concluded. On March 18, 2010, the U.S. Patent and Trademark Office (USPTO) and the Board of Patent Appeals and Interferences ruled in reexamination that the remaining Baxter patent is invalid.

On April 28, 2008, Baxter filed suit in the U.S. District Court for the Northern District of Illinois, Eastern Division (Chicago), styled Baxter International, Inc. and Baxter Healthcare Corporation v. Fresenius Medical Care Holdings, Inc. and Fresenius USA, Inc., Case No. CV 2389, asserting that FMCH's hemodialysis machines infringe four patents issued in 2007 and 2008, all of which are based on one of the patents at issue in the April 2003 Baxter case described above. The new patents expire in April 2011 and relate to trend charts shown on touch screen interfaces and the entry of ultrafiltration profiles (ultrafiltration is the removing of liquid from a patient's body using osmotic pressure). This case is currently stayed pursuant to court order. The Company believes that its hemodialysis machines do not infringe any valid claims of the Baxter patents at issue. All the asserted patents now stand rejected in an ongoing reexamination at the USPTO.

On October 17, 2006, Baxter and DEKA Products Limited Partnership (DEKA) filed suit in the U.S. District Court for the Eastern District of Texas which was subsequently transferred to the Northern District of California, styled Baxter Healthcare Corporation and DEKA Products Limited Partnership v. Fresenius Medical Care Holdings, Inc. d/b/a Fresenius Medical Care North America and Fresenius USA, Inc., Case No. CV 438 TJW. The complaint alleged that FMCH's Liberty™ cycler infringes nine patents owned by or licensed to Baxter. During and after discovery, seven of the asserted patents were dropped from the suit. On July 28, 2010, at the conclusion of the trial, the jury returned a verdict in favor of FMCH finding that the Liberty™ cycler does not infringe any of the asserted claims of the Baxter patents.

A patent infringement action has been pending in Germany between Gambro Industries (Gambro) on the one side and Fresenius Medical Care Deutschland GmbH (D-GmbH) and FMC-AG & Co. KGaA on the other side (hereinafter collectively Fresenius Medical Care). Gambro herein alleged patent infringements by Fresenius Medical Care concerning a patent on a device for the preparation of medical solutions. The District Court of Mannheim rendered a judgment on June 27, 2008 deciding in favor of Gambro and declaring that Fresenius Medical Care has infringed a patent. Accordingly, the court ordered Fresenius Medical Care to pay compensation (to be determined in a separate court proceeding which was initiated by Gambro; after a first hearing in February 2010, the court ordered in May 2010 that the proceedings are stayed until there is a final court decision on the invalidity of the patent) for alleged infringement and to stop offering the alleged patent infringing technology in its original form in Germany. D-GmbH brought an invalidity action in the Federal German Patent Court (BPatG) against Gambro's patent. This case is currently pending with the Federal Court of Justice as the court of appeal. Fresenius Medical Care has also filed an appeal against the District Court's verdict. On January 5, 2009, Gambro enforced such verdict provisionally by way of security. However, preceding such enforcement Fresenius Medical Care had already developed design modifications, being an alternative technical solution, and replaced the alleged patent infringing technology in all of the affected devices. In view of the pending appeal against BPatG's verdict and Fresenius Medical Care's appeal against the District Court's verdict, Fresenius Medical Care continues to believe that the alleged patent infringing technology does not infringe any valid patent claims of Gambro. The patent expired in May 2010, meaning that the provisional enforced injunction is no longer effective.

Other Litigation and Potential Exposures Renal Care Group, Inc. (RCG) is named as a nominal defendant in a complaint originally filed September 13, 2006 in the Chancery Court for the State of Tennessee Twentieth Judicial District at Nashville styled Indiana State District Council of Laborers and Hod Carriers Pension Fund v. Gary Brukardt et al. Following the trial court's dismissal of the complaint, plaintiff's appeal in part, and reversal in part by the appellate court, the cause of action purports to be a class action on behalf of former shareholders of RCG and seeks monetary damages only against the individual former directors of RCG. The individual defendants, however, may have claims for indemnification and reimbursement of expenses against the Company. The Company expects to continue as a defendant in the litigation, which is proceeding toward trial in the Chancery Court, and believes that defendants will prevail.

On July 17, 2007, resulting from an investigation begun in 2005, the United States Attorney filed a civil complaint in the United States District Court for the Eastern District of Missouri (St. Louis) against Renal Group, Inc., its subsidiary RCG Supply Company, and FMCH in its capacity as RCG's current corporate parent. The complaint seeks monetary damages and penalties with respect to issues arising out of the operation of RCG's Method II supply company through 2005, prior to FMCH's acquisition of RCG in 2006. The complaint is styled United States of America ex rel. Julie Williams et al. vs. Renal Care Group, Renal Care Group Supply Company and FMCH. On August 11, 2009, the Missouri District Court granted RCG's motion to transfer venue to the United States District Court for the Middle District of Tennessee (Nashville). On March 22, 2010, the Tennessee District Court entered judgment against defendants for approximately \$ 23 million in damages and interest under the unjust enrichment count of the complaint but denied all relief under the six False Claims Act counts of the complaint. The Company appealed the Tennessee District Court's decision to the United States Court of Appeals for the Sixth Circuit and secured a stay of enforcement of the judgment pending appeal. The United States Attorney filed a cross appeal, but also asked the Tennessee District Court for an indicative or supplemental ruling. On June 23, 2010, the Tennessee District Court issued an indicative ruling to the effect that, if the case were remanded to the District Court, it would expect to enter a judgment under the False Claims Act against the Company for approximately \$ 104 million. The Company believes that RCG's operation of its Method II supply company was in compliance with applicable law, that no relief is due to the United States, and that its position in the litigation will ultimately be sustained.

On November 27, 2007, the United States District Court for the Western District of Texas (El Paso) unsealed and permitted service of two complaints previously filed under seal by a qui tam relator, a former FMCH local clinic employee. The first complaint alleged that a nephrologist unlawfully employed in his practice an assistant to perform patient care tasks that the assistant was not licensed to perform and that Medicare billings by the nephrologist and FMCH therefore violated the False Claims Act. The second complaint alleged that FMCH unlawfully retaliated against the relator by discharging her from employment constructively. The United States Attorney for the Western District of Texas declined to intervene and to prosecute on behalf of the United States. On March 30, 2010, the District Court issued final judgment in favor of defendants on all counts based on a jury verdict rendered on February 25, 2010 and on rulings of law made by the Court during the trial. The plaintiff has appealed from the District Court judgment

On June 25, 2009, FMCH received a subpoena from the U.S. Department of Justice, U.S. Attorney for the District of Massachusetts. The subpoena seeks information relating to the results of certain laboratory tests ordered for patients treated in FMCH's dialysis facilities during the years 2004 through 2009. The Company intends to cooperate fully in the government's investigation.

The Company filed claims for refunds contesting the Internal Revenue Service's (IRS) disallowance of FMCH's civil settlement payment deductions taken by Fresenius Medical Care Holdings, Inc. (FMCH) in prior year tax returns. As a result of a settlement agreement with the IRS, the Company received a partial refund in September 2008 of \$ 37,000, inclusive of interest and preserved our right to pursue claims in the United States

Courts for refunds of all other disallowed deductions. On December 22, 2008, the Company filed a complaint for complete refund in the United States District Court for the District of Massachusetts, styled as Fresenius Medical Care Holdings, Inc. v United States. On June 24, 2010, the court denied FMCH's motion for summary judgment and the litigation is proceeding towards trial.

For the tax year 1997, the Company recognized an impairment of one of our subsidiaries which the German tax authorities disallowed in 2003 at the conclusion of its audit for the years 1996 and 1997. The Company has filed a complaint with the appropriate German court to challenge the tax authority's decision.

The IRS tax audits of FMCH for the years 2002 through 2006 have been completed. The IRS has disallowed all deductions taken during these audit periods related to intercompany mandatorily redeemable preferred shares. The Company has protested the disallowed deductions and will avail itself of all remedies. An adverse determination with respect to the disallowed deductions related to intercompany mandatorily redeemable preferred shares could have a material adverse effect on our results of operations and liquidity. In addition, the IRS proposed other adjustments which have been recognized in the financial statements.

Following Fresenius Medical Care & Co KGaA's Annual General Meeting of Shareholders (AGM) on May 7, 2009, two shareholders challenged, on the basis of alleged insufficient disclosure during the AGM, resolutions taken by the shareholders on (i) the approval of the actions of the General Partner and (ii) the approval of the actions of the members of the Supervisory Board. The Company was of the opinion that the challenges were without merit and defended this litigation vigorously. One of the plaintiffs withdrew his legal challenge in March 2010. The remaining plaintiff withdrew her legal challenge in the beginning of May 2010. Hence, the resolutions adopted on approval of the actions of the General Partner and of the Supervisory Board for fiscal year 2008 have become effective and final.

From time to time, the Company is a party to or may be threatened with other litigation or arbitration, claims or assessments arising in the ordinary course of its business. Management regularly analyzes current information including, as applicable, the Company's defenses and insurance coverage and, as necessary, provides accruals for probable liabilities for the eventual disposition of these matters.

The Company, like other health care providers, conducts its operations under intense government regulation and scrutiny. It must comply with regulations which relate to or govern the safety and efficacy of medical products and supplies, the operation of manufacturing facilities, laboratories and dialysis clinics, and environmental and occupational health and safety. The Company must also comply with the Anti-Kickback Statute, the False Claims Act, the Stark Law, and other federal and state fraud and abuse laws. Applicable laws or regulations may be amended, or enforcement agencies or courts may make interpretations that differ from the Company's interpretations or the manner in which it conducts its business. Enforcement has become a high priority for the federal government and some states.

In addition, the provisions of the False Claims Act authorizing payment of a portion of any recovery to the party bringing the suit encourage private plaintiffs to commence "whistle blower" actions. In May 2009, the scope of the False Claims Act was expanded and additional protections for whistle blowers and procedural provisions to aid whistle blowers' ability to proceed in a False Claims Act case were added. By virtue of this regulatory environment, the Company's business activities and practices are subject to extensive review by regulatory authorities and private parties, and continuing audits, investigative demands, subpoenas, other inquiries, claims and litigation relating to the Company's compliance with applicable laws and regulations. The Company may not always be aware that an inquiry or action has begun, particularly in the case of "whistle blower" actions, which are initially filed under court seal.

The Company operates many facilities throughout the United States. In such a decentralized system, it is often difficult to maintain the desired level of oversight and control over the thousands of individuals employed by many affiliated companies. The Company relies upon its management structure, regulatory and legal resources, and the effective operation of its compliance program to direct, manage and monitor the activities of these employees. On occasion, the Company may identify instances where employees, deliberately or inadvertently, have submitted inadequate or false billings. The actions of such persons may subject the Company and its subsidiaries to liability under the Anti-Kickback Statute, the Stark Law and the False Claims Act, among other laws.

Physicians, hospitals and other participants in the health care industry are also subject to a large number of lawsuits alleging professional negligence, malpractice, product liability, worker's compensation or related claims, many of which involve large claims and significant defense costs. The Company has been and is currently subject to these suits due to the nature of its business and expects that those types of lawsuits may continue. Although the Company maintains insurance at a level which it believes to be prudent, it cannot assure that the coverage limits will be adequate or that insurance will cover all asserted claims. A successful claim against the Company or any of its subsidiaries in excess of insurance coverage could have a material adverse effect upon it and the results of its operations. Any claims, regardless of their merit or eventual outcome, could have a material adverse effect on the Company's reputation and business.

The Company has also had claims asserted against it and has had lawsuits filed against it relating to alleged patent infringements or businesses that it has acquired or divested. These claims and suits relate both to operation of the businesses and to the acquisition and divestiture transactions. The Company has, when appropriate, asserted its own claims, and claims for indemnification. A successful claim against the Company or any of its subsidiaries could have a material adverse effect upon its business, financial condition, and the results of its operations. Any claims, regardless of their merit or eventual outcome, could have a material adverse effect on the Company's reputation and business.

Accrued Special Charge for Legal Matters At December 31, 2001, the Company recorded a pre-tax special charge of \$ 258,159 to reflect anticipated expenses associated with the defense and resolution of pre-Merger tax claims, Merger-related claims, and commercial insurer claims. The costs associated with the Settlement Agreement and settlements with insurers have been charged against this accrual. With the exception of the proposed \$ 115,000 payment under the Settlement Agreement in the Grace Chapter 11 Proceedings, all other matters included in the special charge have been resolved. While the Company believes that its remaining accrual reasonably estimates its currently anticipated costs related to the continued defense and resolution of this matter, no assurances can be given that its actual costs incurred will not exceed the amount of this accrual.

10. Financial Instruments As a global supplier of dialysis services and products in more than 115 countries throughout the world, the Company is faced with a concentration of credit risks due to the nature of the reimbursement systems which are often provided by the governments of the countries in which the Company operates. Changes in reimbursement rates or the scope of coverage could have a material adverse effect on the Company's business, financial condition and results of operations and thus on its capacity to generate cash flow. In the past the Company experienced and also expects in the future generally stable reimbursements for its dialysis services. This includes the balancing of unfavorable reimbursement changes in certain countries with favorable changes in other countries. Due to the fact that a large portion of the Company's reimbursement is provided by public health care organizations and private insurers, the Company expects that most of its accounts receivables will be collectable, albeit somewhat more slowly in the International segment in the immediate future, particularly in countries most severely affected by the global financial crisis.

Non-Derivatives
in \$ thousands Table 25
June 30, 2010 December 31, 2009
Carrying Amount Fair Value Carrying Amount Fair Value
Assets
Cash and cash equivalents 572,851 572,851 301,225 301,225
Short-term investments 122,710 122,710
Accounts Receivable 2,369,154 2,369,154 2,558,795 2,558,795
Liabilities
Accounts payable 475,863 475,863 639,836 639,836
Short-term borrowings 410,057 410,057 316,344 316,344
Short-term borrowings from related parties 8,893 8,893 10,440 10,440
Long term debt, excluding 2006 Senior Credit Agreement,
Euro Notes and Senior Notes 397,837 397,837 282,051 282,051
2006 Senior Credit Agreement 3,375,326 3,300,894 3,522,040 3,429,470
Trust Preferred Securities 592,478 612,765 656,096 688,026
Euro Notes 245,420 253,626 288,120 299,621
Senior Notes 796,726 822,512 493,344 498,750

Non-Derivative Financial Instruments The following table presents the carrying amounts and fair values of the Company's non-derivative financial instruments at June 30, 2010, and December 31, 2009.

The carrying amounts in the table are included in the consolidated balance sheet under the indicated captions or in the case of long-term debt, as noted in the captions shown in Note 6.

The significant methods and assumptions used in estimating the fair values of non-derivative financial instruments are as follows:

Cash and cash equivalents are stated at nominal value which equals the fair value.

Short-term financial instruments such as accounts receivable, short-term investments, accounts payable and short-term borrowings are valued at their carrying amounts, which are reasonable estimates of the fair value due to the relatively short period to maturity of these instruments.

The fair values of the major long-term financial liabilities are calculated on the basis of market information. Instruments for which market quotes are available are measured using these quotes. The fair values of the other long-term financial liabilities are calculated at the present value of the respective future cash flows. To determine these present values, the prevailing interest rates and credit spreads for the Company as of the balance sheet date are used.

Derivative Financial Instruments The Company is exposed to market risk from changes in interest rates and foreign exchange rates. In order to manage the risk of interest rate and currency exchange rate fluctuations, the Company enters into various hedging transactions by means of derivative instruments with highly rated financial institutions as authorized by the Company's General Partner. On a quarterly basis the Company performs an assessment of its counterparty credit risk. The Company currently considers this risk to be

low. The Company's policy, which has been consistently followed, is that financial derivatives be used only for the purpose of hedging foreign currency and interest rate exposure.

In certain instances, the Company enters into derivative contracts that do not qualify for hedge accounting but are utilized for economic purposes (economic hedges). The Company does not use financial instruments for trading purposes.

Foreign Exchange Risk Management The Company conducts business on a global basis in various currencies, though its operations are mainly in Germany and the United States. For financial reporting purposes, the Company has chosen the U.S. dollar as its reporting currency. Therefore, changes in the rate of exchange between the U.S. dollar and the local currencies in which the financial statements of the Company's international operations are maintained affect its results of operations and financial position as reported in its consolidated financial statements.

The Company's exposure to market risk for changes in foreign exchange rates relates to transactions such as sales and purchases. The Company has significant amounts of sales of products invoiced in euro from its European manufacturing facilities to its other international operations and, to a lesser extent, sales of products invoiced in other non-functional currencies. This exposes the subsidiaries to fluctuations in the rate of exchange between the euro and the currency in which their local operations are conducted. For the purpose of hedging existing and foreseeable foreign exchange transaction exposures the Company enters into foreign exchange forward contracts and, on a small scale, foreign exchange options. As of June 30, 2010 the Company had no foreign exchange options.

Changes in the effective portion of fair value of foreign exchange forward contracts designated and qualifying as cash flow hedges of forecasted product purchases and sales are reported in accumulated other comprehensive income (loss) (AOCI) when they qualify for hedge accounting. Additionally, in connection with intercompany loans in foreign currency, the Company uses foreign exchange swaps thus assuring that no foreign exchange risks arise from those loans, which, if they qualify for hedge accounting, are also reported in AOCI. These amounts recorded in AOCI are subsequently reclassified into earnings as a component of cost of revenues for those contracts that hedge product purchases or SG&A for those contracts that hedge loans, in the same period in which the hedged transaction affects earnings. The notional amounts of foreign exchange contracts in place that are designated and qualify as cash flow hedges totaled \$ 859,555 and \$ 1,076,217 at June 30, 2010 and December 31, 2009, respectively.

The Company also enters into derivative contracts of forecasted product purchases and sales and for intercompany loans in foreign currency that do not qualify for hedge accounting but are utilized for economic hedges as defined above. In these cases, the change in value of the economic hedge is recorded in the income statement and usually offsets the change in value recorded in the income statement for the underlying asset or liability. The notional amounts of economic hedges that do not qualify for hedge accounting totaled \$ 893,978 and \$ 750,812 at June 30, 2010 and December 31, 2009, respectively.

Interest Rate Risk Management The Company enters into derivatives, particularly interest rate swaps and to a certain extent, interest rate options, to protect against the risk of rising interest rates. These interest rate derivatives are designated as cash flow hedges. The majority of the interest rate swap agreements effectively convert the major part of payments based on variable interest rates applicable to the Company's 2006 Senior Credit Agreement denominated in U.S. dollars into payments at a fixed interest rate. The remaining interest rate swaps have been entered into in anticipation of future debt issuances.

As of June 30, 2010 and December 31, 2009, the notional amounts of interest rate swaps in place were \$ 3,175,000 and \$ 2,400,000, respectively.

Derivative Financial Instruments Valuation The following table shows the Company's derivatives at June 30, 2010 and December 31, 2009.

derivatives
in \$ thousands Table 26
December 31, 2009
Assets2 June 30, 2010 Liabilities2
Assets2
Liabilities2
Derivatives in cash flow hedging relationships1
Current
Foreign exchange contracts 1,755 (118,000) 8,899 (9,251)
Interest rate contracts ( Dollar) (68,753) (305)
Interest rate contracts (Yen) (1)
Non-current
Foreign exchange contracts 18 (1,055) 5,284 (830)
Interest rate contracts ( Dollar) (90,074) (105,810)
Interest rate contracts (Yen) (3)
total 1,773 (277,883) 14,183 (116,199)
Derivatives not designated as hedging instruments1
Current
Foreign exchange contracts 2,283 (28,055) 7,696 (6,217)
Non-current
Foreign exchange contracts 8 9
total 2,291 (28,055) 7,705 (6,217)

1 As of June 30, 2010 and December 31, 2009, the valuation of the Company's derivatives was determined using Significant Other Observable Inputs (Level 2) in accordance with the fair value hierarchy levels established in U.S. GAAP.

2 Derivative instruments are marked to market each reporting period resulting in carrying amounts being equal to fair values at reporting date.

The carrying amounts for the current portion of derivatives indicated as assets in the table above are included in Prepaid expenses and other current assets in the Consolidated Balance Sheets while the current portion of those indicated as liabilities are included in Accrued expenses and other current liabilities. The non-current portions indicated as assets or liabilities are included in the Consolidated Balance Sheets in Other assets or Other liabilities, respectively.

The significant methods and assumptions used in estimating the fair values of derivative financial instruments are as follows:

The fair value of interest rate swaps is calculated by discounting the future cash flows on the basis of the market interest rates applicable for the remaining term of the contract as of the balance sheet date. To determine the fair value of foreign exchange forward contracts, the contracted forward rate is compared to the current forward rate for the remaining term of the contract as of the balance sheet date. The result is then discounted on the basis of the market interest rates prevailing at the balance sheet date for the applicable currency.

The Company includes its own credit risk for financial instruments deemed liabilities and counterpartycredit risks for financial instruments deemed assets when measuring the fair value of derivative financial instruments.

Table 27 Consolidated financial statements
Amount of Gain or (Loss )
Location of
Recognized in OCI on Derivative
(Gain) or Lossre
classified from
(Effective Portion)
AOCI in Income
fied from AOCI in Income
(Effective Portion) for the three
months ended June 30,
(Effective Portion) 2009
Interest
income/ (33)
1 5 expense
Costs of
(5,159) Revenue 1,889 (3,499)
19,378 1,889 (3,532)
June 30, 2010
(52,711)
(22,130)
(74,840)
June 30, 2009
24,532
expense
Interest
income/
Amount of (Gain) or Loss reclassi
2010
in \$ thousands the effect of derivatives on the
Consolidated financial statements
Table 27
Location of (Gain) or Loss Recognized
in Income on Derivative
Amount of (Gain) or Loss
Recognized in Income on Derivatives
for the three months ended June 30,
2010 2009
Derivatives not Designated as Hedging Instruments
Selling,
Foreign exchange contracts general and administrative expense 42,864 (3,795)
Interest income/expense (9,247) (690)
total 33,617 (4,485)

The Company expects to recognize \$ 8,244 of losses deferred in accumulated other comprehensive income at March 31, 2010, in earnings during the next twelve months.

As of June 30, 2010, the Company had foreign exchange derivatives with maturities of up to 29 months and interest rate swaps with maturities of up to 26 months.

11. Business Segment Information The Company has identified three business segments, North America, International, and Asia Pacific, which were determined based upon how the Company manages its businesses. All segments are primarily engaged in providing dialysis care services and manufacturing and distribution products and equipment for the treatment of ESRD. In the U.S., the Company is also engaged in performing clinical laboratory testing and providing inpatient dialysis services and other services under contract to hospitals. The Company has aggregated the International and Asia Pacific operating segments as "International". The segments are aggregated due to their similar economic characteristics. These characteristics include the same services provided and products sold, the same type patient population, similar methods of distribution of products and services and similar economic environments.

Management evaluates each segment using a measure that reflects all of the segment's controllable revenues and expenses. Management believes that the most appropriate measure in this regard is operating income which measures the Company's source of earnings. Financing is a corporate function, which the Company's segments do not control. Therefore, the Company does not include interest expense relating to financing as a segment measure. Similarly, the Company does not allocate "corporate costs", which relate primarily to certain headquarters overhead charges, including accounting and finance, professional services, etc., because the Company believes that these costs are also not within the control of the individual segments. In addition, certain acquisitions and intangible assets are not allocated to a segment but are accounted for as "corporate". The Company also regards income taxes to be outside the segment's control.

Information pertaining to the Company's business segments for the three-month periods ended March 31, 2010 and 2009 is set forth below.

Business segment information
in \$ thousands Table 28
North America International Segment Total Corporate Total
Three months ended June 30, 2010
Net revenue external customers 2,026,582 919,524 2,946,106 93 2,946,199
Inter-segment revenue 1,263 22,053 23,316 (23,316)
Revenue 2,027,845 941,577 2,969,422 (23,223) 2,946,199
Depreciation and amortization (71,221) (47,348) (118,569) (2,338) (120,907)
Operating Income 330,209 173,095 503,304 (38,626) 464,678
Capital expenditures,
acquisitions and investments 86,955 106,361 193,316 135,086 328,402
Three months ended June 30, 2009
Net revenue external customers 1,876,347 887,071 2,763,418 151 2,763,569
Inter-segment revenue 769 21,467 22,236 (22,236)
Revenue 1,877,116 908,538 2,785,654 (22,085) 2,763,569
Depreciation and amortization (64,762) (43,420) (108,182) (2,189) (110,371)
Operating Income 297,495 153,548 451,043 (33,406) 417,637
Capital expenditures,
acquisitions and investments 106,149 80,318 186,467 315 186,782
Six months ended June 30, 2010
Net revenue external customers 3,986,270 1,841,747 5,828,017 311 5,828,328
Inter-segment revenue 1,828 43,152 44,980 (44,980)
Total Net Revenue 3,988,098 1,884,899 5,872,997 (44,669) 5,828,328
Depreciation and amortization (142,924) (97,718) (240,642) (4,723) (245,365)
Operating Income 636,426 324,025 960,451 (72,284) 888,167
Segment assets 11,281,830 3,948,045 15,229,875 769,689 15,999,564
Capital expenditures,
acquisitions and investments1 179,806 199,144 378,950 138,932 517,882
Six months ended June 30, 2009
Net revenue external customers 3,650,159 1,672,914 5,323,073 306 5,323,379
Inter-segment revenue 1,233 38,993 40,226 (40,226)
total net Revenue 3,651,392 1,711,907 5,363,299 (39,920) 5,323,379
Depreciation and amortization (128,455) (83,173) (211,628) (4,214) (215,842)
Operating Income 569,431 300,335 869,766 (56,287) 813,479
Segment assets 11,051,728 3,913,502 14,965,230 369,845 15,335,075
Capital expenditures,
acquisitions and investments2 182,600 151,978 334,578 770 335,348

1 International and Corporate acquisitions exclude \$ 8,884 and \$ 2,125, respectively, of non-cash acquisitions for 2010.

2 International acquisitions exclude \$ 1,828 of non-cash acquisitions for 2009.

12. Supplementary Cash Flow Information The following additional information is provided with respect to the consolidated statements of cash flows:

supplementary cash flow information
in \$ thousands Table 29
Six months ended June 30,
2010 2009
Supplementary cash flow information
Cash paid for interest 143,222 166,520
Cash paid for income taxes1 261,695 214,724
Cash inflow for income taxes from stock option exercises 2,378 2,386
Supplemental disclosures of cash flow information
Details for acquisitions:
Assets acquired (186,560) (97,004)
Liabilities assumed 11,303 6,227
Noncontrolling interest 5,741 13,585
Notes assumed in connection with acquisition 11,009 1,828
cash paid (158,507) (75,364)
Less cash acquired 1,678 4,005
Net cash paid for acquisitions (156,829) (71,359)

1 Net of tax refund

Events occurring after the balance sheet date 51

No significant activities have taken place since the balance sheet date June 30, 2010, which have a material impact in any way on the key figures presented and business earnings.

corporate governance

The personally liable shareholder, represented by the Managing Board of Fresenius Medical Care Management AG, and the Supervisory Board of FMC-AG & Co. KGaA have issued a compliance declaration pursuant to § 161 of the German Stock Corporation Act (AktG). The Company has frequently made this declaration available to the public by pushing it on its website: www.fmc-ag.com.

responsibility statement

"To the best of our knowledge, and in accordance with the applicable reporting principles for interim financial reporting, the interim consolidated financial statements give a true and fair view of the assets, liabilities, financial position and profit or loss of the Fresenius Medical Care-Group, and the interim management report of the group includes a fair review of the development and performance of the business and the position of the group, together with a description of the principal opportunities and risks associated with the expected development of the group for the remaining months of the financial year."

August 3, 2010 Fresenius Medical Care AG & Co. KGaA

Represented by the General Partner Fresenius Medical Care Management AG

Dr. B. Lipps R. Powell M. Brosnan R. Fusté

Dr. E. Gatti Dr. R. Runte K. Wanzek

Fresenius Medical Care 2010

Calendar and contact

52

Calendar 2010

September 1 – 2, 2010 Capital Markets Day

november 2, 2010 Report on Nine Months 2010

Calendar 2011

February 23, 2011 Report on Full Year 2010

May 4, 2011 Report on First Quarter 2011

May 12, 2011 Annual General Meeting 2011

May 13, 2011 Dividend Payment

August 2, 2011 Report on First Half 2011

November 2, 2011 Report on Nine Months 2011

Please notice that these dates might be subject to change.

Contact

Fresenius Medical Care AG & CO. KGaA investor relations Else-Kröner-Str. 1 61352 Bad Homburg, Germany Internet: www.fmc-ag.com

Oliver Maier

Phone: + 49 6172 609 26 01 Fax: + 49 6172 609 23 01 E-Mail: [email protected]

North America

Terry L. Morris Phone: + 1 800 948 25 38 Fax: + 1 615 345 56 05 E-Mail: [email protected]

This interim report is also available in German.

Annual reports, interim reports and further information on the Company is also available on our website. Please visit us at www.fmc-ag.com

For printed material, please contact Investor Relations.

Published by Fresenius Medical Care AG & Co. KGaA Investor Relations

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