FDA Inspection 1248982 — Angela L. Gentile, M.D.

Angela L. Gentile, M.D. — FEI 3031092081

The FDA completed an inspection of Angela L. Gentile, M.D. on August 23, 2024 in Buenos Aires. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 23, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Buenos Aires (Argentina)

Additional Details

Clinical Investigator (CI)