FDA Inspection 1245096 — Kevin D. Benson MD

Kevin D. Benson MD — FEI 3015886776

The FDA completed an inspection of Kevin D. Benson MD on Jul 25, 2024 in Sioux Falls, SD. 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
Jul 25, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sioux Falls, SD (United States)

Additional Details

Clinical Investigator (CI)