FDA Inspection 965779 — Kenneth Yamamura, MD

Kenneth Yamamura, MD — FEI 3011936073

The FDA completed an inspection of Kenneth Yamamura, MD on Apr 11, 2016 in Tampa, 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
Apr 11, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tampa, FL (United States)

Additional Details

Clinical Investigator (CI)