FDA Inspection 1039565 — Kelly H. Roy, MD

Kelly H. Roy, MD — FEI 3014002944

The FDA completed an inspection of Kelly H. Roy, MD on January 24, 2018 in Phoenix, AZ. 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
January 24, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)