FDA Inspection 755779 — Edward Fry, MD

Edward Fry, MD — FEI 3008629052

The FDA completed an inspection of Edward Fry, MD on Dec 5, 2011 in Indianapolis, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 5, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Clinical Investigator (CI)