FDA Inspection 1048857 — Harvey Serota, M.D.

Harvey Serota, M.D. — FEI 3014249021

The FDA completed an inspection of Harvey Serota, M.D. on Apr 3, 2018 in Saint 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
Apr 3, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)