FDA Inspection 956453 — Alexander Coon, MD

Alexander Coon, MD — FEI 3011901321

The FDA completed an inspection of Alexander Coon, MD on January 14, 2016 in Tucson, 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 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tucson, AZ (United States)

Additional Details

Clinical Investigator (CI)