FDA Inspection 1325110 — Dr. Michael Montana, M.D.

Dr. Michael Montana, M.D. — FEI 3043619192

The FDA completed an inspection of Dr. Michael Montana, M.D. on Jun 18, 2026 in St. Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 18, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
St. Louis, MO (United States)

Additional Details

Clinical BA/BE