FDA Inspection 1009806 — Ajanta Pharma Ltd.
The FDA completed an inspection of Ajanta Pharma Ltd. on February 7, 2017 in Paithan. 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
- February 7, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Paithan (India)