FDA Inspection 605928 — Gary D Monheit, MD

Gary D Monheit, MD — FEI 1038570

The FDA completed an inspection of Gary D Monheit, MD on Aug 6, 2009 in Birmingham, AL. 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
Aug 6, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Birmingham, AL (United States)

Additional Details

Clinical Investigator (CI)