FDA Documents of Actelion Pharmaceuticals U.S., Inc.
Actelion Pharmaceuticals U.S., Inc. is an organization that has been audited by the FDA 9 times between 2003 and 2024 across all 3 sites.
Documents
FDA 483 Actelion Pharmaceuticals U.S | Feb 2014
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Issued on: Feb 12, 2014
Human Drug Form 483
FDA 483 Actelion Pharmaceuticals U.S., Inc., South San Francisco | 2016
Out-of-stock
Issued on: Sep 21, 2016
Human Drug Form 483
FDA 483 Actelion Pharmaceuticals U.S., Inc., South San Francisco | 2011
Out-of-stock
Issued on: Jul 21, 2011
Human Drug Form 483
FDA 483 Actelion Pharmaceuticals U.S., Inc., South San Francisco | 2009
Out-of-stock
Issued on: Jul 20, 2009
Human Drug Form 483
FDA Investigators(10)
- Thea C. Grome, FDA Investigator
- Lucila B. Nwatu, FDA Investigator
- Anh Lac, FDA Investigator
- Lance M. De Souza, FDA Investigator
- Daniel J. Roberts, FDA Investigator
- De Souza, Lance M, FDA Investigator
- William V. Millar, FDA Investigator
- Kevin P. Foley, FDA Investigator
- Darlene B. Almogela, FDA Investigator
- Maida Henesian, FDA Investigator