FDA Inspection 934309 — Korenblat, Dr Phillip E
The FDA completed an inspection of Korenblat, Dr Phillip E on Jul 9, 2015 in Creve Coeur, MO. 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
- Jul 9, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Creve Coeur, MO (United States)
Additional Details
Clinical Investigator (CI)