FDA Inspection 577813 — Actavis Totowa LLC
The FDA completed an inspection of Actavis Totowa LLC on March 31, 2009 in Totowa, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 31, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Totowa, NJ (United States)