CLOSEOUT LETTER
Fresenius Kabi USA, LLC
- Recipient:
- Fresenius Kabi USA, LLC
United States
- Issuing Office:
United States
Division of Pharmaceutical Quality Operations I | |
July 26, 2017
John Ducker, President
Fresenius Kabi USA, LLC
Three Corporate Drive
Lake Zurich, Illinois 6004 7
Dear Mr. Ducker:
The Food and Drug Administration has completed an evaluation of your firm's corrective actions in response to our Warning Letter [NYK-2012-14 dated February 22, 2012]. Based on our evaluation, it appears that you have addressed the violation(s) contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.
This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.
/S/
CDR Frank Verni, R.Ph.
Compliance Officer
U.S. Food and Drug Administration
New York District Office
Pharmaceutical Quality I Compliance Branch (PHRMl-CB)
cc (via email):
• Michael Schonhofen, President, Phannaceutical Division
• Steve Nowicki, Senior Vice President - Global Operations North America
• Anne Huffman, Vice President, Quality Assurance - Plant Operations
Office of Pharmaceutical Quality Operations. Division of Pharmaceutical Quality Operations I
New England District Office: One Montvale Avenue, 4th Floor Stoneham, MA 02180-3500
T- (781) 587-7500 F- (781) 587-7556
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Baltimore District Office: 6000 Metro Drive, Suite 101 Baltimore, MD 21215
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