FDA Inspection 978926 — Apotex Pharmachem India Pvt Ltd.
The FDA completed an inspection of Apotex Pharmachem India Pvt Ltd. on June 3, 2016 in Bangalore. 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
- June 3, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Bangalore (India)