FDA Inspection 621388 — Gary D Monheit, MD

Gary D Monheit, MD — FEI 1038570

The FDA completed an inspection of Gary D Monheit, MD on Oct 8, 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 8, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Birmingham, AL (United States)

Additional Details

Clinical Investigator (CI)