Allergan Form 483 Details
Form 483Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 2024601.
Allergan
Goleta, California, United States
Issue DateAugust 22, 2012
FEI Number2024601
CountryUnited States
Status
1 Related Warning LetterProduct Type
Devices