FDA Documents of Gruppo Lepetit Srl
Gruppo Lepetit Srl is an organization that has been audited by the FDA 7 times between 2000 and 2012 across all 1 sites.
Documents
FDA 483 Gruppo Lepetit Srl, Anagni | 2012
Out-of-stock
Issued on: Mar 22, 2012
Human Drug Form 483
FDA 483 Gruppo Lepetit Srl, Anagni | 2011
Out-of-stock
Issued on: Jun 23, 2011
Medical Devices & Rad Health Form 483
FDA 483 Gruppo Lepetit Srl, Anagni | 2008
Out-of-stock
Issued on: Sep 16, 2008
Human Drug Form 483
FDA 483 Gruppo Lepetit Srl, Anagni | 2005
Out-of-stock
Issued on: Sep 29, 2005
Medical Devices & Rad Health Form 483
FDA 483 Gruppo Lepetit Srl, Anagni | 2002
Out-of-stock
Issued on: Dec 13, 2002
Human Drug Form 483
FDA 483 Gruppo Lepetit Srl, Anagni | 2000
Out-of-stock
Issued on: May 8, 2000
Human Drug Form 483
FDA Investigators(11)
- Temar Q. Williams, FDA Investigator
- Denise M. Digiulio, FDA Investigator
- Donna L. Besone, FDA Investigator
- Kristy A. Zielny, FDA Investigator
- Barbara D. Paul, FDA Investigator
- Richard K. Vogel, FDA Investigator
- James A. Beaulieu, FDA Investigator
- David M. Beltran, FDA Investigator
- Jose A. Cruz Gonzalez, FDA Investigator
- Gerald B. Seaborn, FDA Investigator
- Cruz Gonzalez, Jose A, FDA Investigator