FDA Inspection 1048732 — Rogelio Amisola MD

Rogelio Amisola MD — FEI 3014145960

The FDA completed an inspection of Rogelio Amisola MD on Mar 29, 2018 in Dayton, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 29, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Dayton, OH (United States)

Additional Details

Clinical Investigator (CI)