FDA Documents of Novartis Pharma Produktions GmbH
Novartis Pharma Produktions GmbH is an organization that has been audited by the FDA 13 times between 2001 and 2023 across all 2 sites.
Documents
FDA 483 Novartis Pharma Produktions GmbH, Wehr | 2011
Out-of-stock
Issued on: Sep 15, 2011
Human Drug Form 483
FDA 483 Novartis Pharma Produktions GmbH, Wehr | 2006
Out-of-stock
Issued on: May 11, 2006
Human Drug Form 483
FDA 483 Novartis Pharma Produktions GmbH, Wehr | 2003
Out-of-stock
Issued on: Oct 9, 2003
Human Drug Form 483
FDA 483 Novartis Pharma Produktions GmbH, Wehr | 2002
Out-of-stock
Issued on: Mar 8, 2002
Human Drug Form 483
FDA Investigators(13)
- Jacob G. Lutz, FDA Investigator
- Michael H. Tollon, FDA Investigator
- Saied A. Asbagh, FDA Investigator
- Azza Talaat, FDA Investigator
- Steven D. Kehoe, FDA Investigator
- Maya M. Davis, FDA Investigator
- Laurie B. Frazier, FDA Investigator
- Bruce H. McCullough, FDA Investigator
- Kevin D. Kallander, FDA Investigator
- Paul L. Bellamy, FDA Investigator
- Robert D. Tollefsen, FDA Investigator
- Rafael Nevarez Nieves, FDA Investigator
- Nevarez Nieves, Rafael, FDA Investigator