FDA Documents of Kiel Laboratories Inc
Kiel Laboratories Inc is an organization that has been audited by the FDA 13 times between 2001 and 2017 across all 2 sites.
Documents
FDA 483 Kiel Laboratories Inc, Gainesville | 2006
Out-of-stock
Issued on: Aug 14, 2006
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2005
Out-of-stock
Issued on: Dec 22, 2005
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2004
Out-of-stock
Issued on: Sep 9, 2004
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2004
Out-of-stock
Issued on: Jan 8, 2004
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2003
Out-of-stock
Issued on: May 27, 2003
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2002
Out-of-stock
Issued on: Sep 17, 2002
Human Drug Form 483
FDA 483 Kiel Laboratories Inc, Gainesville | 2001
Out-of-stock
Issued on: Jul 26, 2001
Human Drug Form 483
FDA Investigators(12)
- Susan O. Oladeji, FDA Investigator
- Tajah L. Blackburn, FDA Investigator
- Tamara J. Henderson, FDA Investigator
- Reba A. Gates, FDA Investigator
- Penny H. McCarver, FDA Investigator
- Gabriel R. McLemore, FDA Investigator
- Burnell M. Henry, FDA Investigator
- Luis M. Burgos Medero, FDA Investigator
- Carlos A. Ortiz, FDA Investigator
- Burgos Medero, Luis M, FDA Investigator
- Leah M. Andrews, FDA Investigator
- Jacqueline D. Mitchell, FDA Investigator