FDA Documents of Neopharm Laboratories
Neopharm Laboratories is an organization that has been audited by the FDA 11 times between 2000 and 2014 across all 2 sites.
Documents
FDA 483 Neopharm Laboratories, Blainville | 2010
Out-of-stock
Issued on: Feb 16, 2010
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2007
Out-of-stock
Issued on: Jun 7, 2007
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2006
Out-of-stock
Issued on: Mar 24, 2006
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2004
Out-of-stock
Issued on: Sep 30, 2004
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2002
Out-of-stock
Issued on: Nov 15, 2002
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2002
Out-of-stock
Issued on: Nov 7, 2002
Human Drug Form 483
FDA 483 Neopharm Laboratories, Blainville | 2000
Out-of-stock
Issued on: Feb 1, 2000
Human Drug Form 483
FDA Investigators(13)
- Truong X. Nguyen, FDA Investigator
- Bonita S. Chester, FDA Investigator
- Carla A. Norris, FDA Investigator
- Rebecca Rodriguez, FDA Investigator
- Dana M. Klimavicz, FDA Investigator
- Mural B. Gavini, FDA Investigator
- Barbara J. Breithaupt, FDA Investigator
- Susan F. Laska, FDA Investigator
- Sarah M. Forney, FDA Investigator
- Edwin Martinez, FDA Investigator
- Charles M. Edwards, FDA Investigator
- Raymond T. Oji, FDA Investigator
- Eric S. Weilage, FDA Investigator