FDA Inspection 889295 — Kevin D. Accola, MD

Kevin D. Accola, MD — FEI 3010393493

The FDA completed an inspection of Kevin D. Accola, MD on Aug 1, 2014 in Orlando, FL. 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
Aug 1, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Orlando, FL (United States)

Additional Details

Clinical Investigator (CI)