FDA Warning Letter — Akorn, Inc.
The FDA took a Warning Letter action against Akorn, Inc. on October 2, 2012 (Gurnee, IL). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Akorn, Inc.
- Date
- October 2, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Center
- CDER
- Location
- Gurnee, IL (United States)