FDA Inspection 948221 — Jubilant Pharmova Limited
The FDA completed an inspection of Jubilant Pharmova Limited on Oct 16, 2015 in Mysore. 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
- Oct 16, 2015
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Mysore (India)