FDA Inspection 1099773 — Armodios M. Hatzidakis, M.D.

Armodios M. Hatzidakis, M.D. — FEI 3015471365

The FDA completed an inspection of Armodios M. Hatzidakis, M.D. on July 11, 2019 in Denver, CO. 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
July 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Denver, CO (United States)

Additional Details

Clinical Investigator (CI)