FDA Inspection 1008794 — Kelly Hunt, MD

Kelly Hunt, MD — FEI 3013222094

The FDA completed an inspection of Kelly Hunt, MD on March 31, 2017 in Houston, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Houston, TX (United States)

Additional Details

Clinical Investigator (CI)