FDA Inspection 1044875 — Dr Vance Thompson

Dr Vance Thompson — FEI 3000177207

The FDA completed an inspection of Dr Vance Thompson on Mar 1, 2018 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
Mar 1, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sioux Falls, SD (United States)

Additional Details

Clinical Investigator (CI)