FDA Inspection 780775 — David E. Geller

David E. Geller — FEI 3009425483

The FDA completed an inspection of David E. Geller on April 30, 2012 in Orlando, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 30, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Orlando, FL (United States)

Additional Details

Clinical Investigator (CI)