FDA Inspection 775866 — Marco Cioppi, MD

Marco Cioppi, MD — FEI 3009429880

The FDA completed an inspection of Marco Cioppi, MD on Mar 14, 2012 in Huntsville, AL. 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
Mar 14, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Huntsville, AL (United States)

Additional Details

Clinical Investigator (CI)