FDA Inspection 722033 — Actavis South Atlantic LLC
The FDA completed an inspection of Actavis South Atlantic LLC on Apr 28, 2011 in Sunrise, FL. 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
- Apr 28, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sunrise, FL (United States)