FDA Inspection 1208745 — Manish Hathila, M.D.

Manish Hathila, M.D. — FEI 3026006209

The FDA completed an inspection of Manish Hathila, M.D. on May 24, 2023 in Ahmedabad. 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 24, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ahmedabad (India)

Additional Details

Clinical BA/BE