FDA Inspection 1302490 — Kelly H. Roy, MD

Kelly H. Roy, MD — FEI 3014002944

The FDA completed an inspection of Kelly H. Roy, MD on January 30, 2026 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 30, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)