FDA Inspection 948048 — Akorn Inc
The FDA completed an inspection of Akorn Inc on November 10, 2015 in Vernon Hills, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 10, 2015
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Vernon Hills, IL (United States)