FDA Inspection 1099752 — Randy I. Cooper, MD

Randy I. Cooper, MD — FEI 3015421173

The FDA completed an inspection of Randy I. Cooper, MD on August 14, 2019 in Tempe, 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
August 14, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tempe, AZ (United States)

Additional Details

Clinical Investigator (CI)