FDA Inspection 994679 — Actavis Elizabeth LLC
The FDA completed an inspection of Actavis Elizabeth LLC on Dec 5, 2016 in Elizabeth, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 5, 2016
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Elizabeth, NJ (United States)