FDA Inspection 878592 — Fausto Devecchi, M.D.

Fausto Devecchi, M.D. — FEI 3010405408

The FDA completed an inspection of Fausto Devecchi, M.D. on Apr 11, 2014 in Fort Wayne, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fort Wayne, IN (United States)

Additional Details

Clinical Investigator (CI)