FDA Inspection 1208162 — Keyur M. Brahme, MD

Keyur M. Brahme, MD — FEI 3015850247

The FDA completed an inspection of Keyur M. Brahme, MD on May 30, 2023 in Vadodara. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 30, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Vadodara (India)

Additional Details

Clinical BA/BE