FDA Inspection 1030256 — Gensynth Laboratories Private Limited
The FDA completed an inspection of Gensynth Laboratories Private Limited on September 21, 2017 in Sangareddy District, Medak. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 21, 2017
- Fiscal Year
- 2017
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sangareddy District, Medak (India)