FDA Inspection 1320248 — Dr. Vendel Kemeny M.D., Ph.D.
The FDA completed an inspection of Dr. Vendel Kemeny M.D., Ph.D. on May 29, 2026 in Budapest. 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
- May 29, 2026
- Fiscal Year
- 2026
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Budapest (Hungary)
Additional Details
Clinical BA/BE