FDA Inspection 1089074 — Arthur Berman, D.O.

Arthur Berman, D.O. — FEI 3015216411

The FDA completed an inspection of Arthur Berman, D.O. on April 23, 2019 in Largo, FL. 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
April 23, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Largo, FL (United States)

Additional Details

Clinical Investigator (CI)