FDA Inspection 930362 — Abram H. Burgher, MD

Abram H. Burgher, MD — FEI 3011564468

The FDA completed an inspection of Abram H. Burgher, MD on May 29, 2015 in Peoria, 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
May 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Peoria, AZ (United States)

Additional Details

Clinical Investigator (CI)