FDA Inspection 1050212 — Dr. Harvey DuBiner

Dr. Harvey DuBiner — FEI 3014213252

The FDA completed an inspection of Dr. Harvey DuBiner on Apr 17, 2018 in Morrow, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Morrow, GA (United States)

Additional Details

Clinical Investigator (CI)