FDA Inspection 1280311 — David E. Kandzari, M.D.

David E. Kandzari, M.D. — FEI 3010209049

The FDA completed an inspection of David E. Kandzari, M.D. on August 15, 2025 in Atlanta, GA. 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 15, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Clinical Investigator (CI)