Akorn, Inc. 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 3003102962.
Akorn, Inc.
Gurnee, Illinois, United States
Issue DateNovember 10, 2009
FEI Number3003102962
CountryUnited States
Status
2 Related Warning LettersProduct Type
Drugs