FDA Inspection 1050360 — Kirk Voelker, MD

Kirk Voelker, MD — FEI 3009339545

The FDA completed an inspection of Kirk Voelker, MD on Apr 12, 2018 in Sarasota, 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 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Sarasota, FL (United States)

Additional Details

Clinical Investigator (CI)