FDA Inspection 1010713 — Angela C. Silber MD

Angela C. Silber MD — FEI 3013156678

The FDA completed an inspection of Angela C. Silber MD on April 7, 2017 in Akron, OH. 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 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Akron, OH (United States)

Additional Details

Clinical Investigator (CI)