FDA Inspection 1071165 — Dr. Sandeep Kumar Gupta
The FDA completed an inspection of Dr. Sandeep Kumar Gupta on Aug 31, 2018 in Lucknow. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 31, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Lucknow (India)
Additional Details
Clinical Investigator (CI)