FDA Documents of Allergan
Allergan is an organization that has been audited by the FDA 21 times between 2000 and 2014 across all 4 sites.
Documents
FDA 483 Allergan, Goleta | 2012
Out-of-stock
Issued on: Aug 22, 2012
Medical Devices & Rad Health Form 483
FDA 483 Allergan, Arklow, County Wicklow | 2007
Out-of-stock
Issued on: Sep 20, 2007
Medical Devices & Rad Health Form 483
FDA 483 Allergan, Arklow, County Wicklow | 2005
Out-of-stock
Issued on: Nov 10, 2005
Medical Devices & Rad Health Form 483
FDA 483 Allergan, Goleta | 2005
Out-of-stock
Issued on: Feb 18, 2005
Medical Devices & Rad Health Form 483
FDA 483 Allergan, Goleta | 2002
Out-of-stock
Issued on: Apr 5, 2002
Medical Devices & Rad Health Form 483
FDA 483 Allergan, Goleta | 2000
Out-of-stock
Issued on: Apr 14, 2000
Medical Devices & Rad Health Form 483
FDA Investigators(13)
- James R. Fleckenstein, FDA Investigator
- Kelvin Cheung, FDA Investigator
- Leonard H. Lavi, FDA Investigator
- Vickie L. Anderson, FDA Investigator
- Jesse A. Vazquez, FDA Investigator
- Patricia A. McIlroy, FDA Investigator
- Paul R. Whitby, FDA Investigator
- Selene T. Torres, FDA Investigator
- George T. Allen, FDA Investigator
- Dannie E. Rowland, FDA Investigator
- Jocelyn E. Massey, FDA Investigator
- William R. Bowman, FDA Investigator
- Allen F. Hall, FDA Investigator