FDA Inspection 1134857 — Peter Gottlieb, MD

Peter Gottlieb, MD — FEI 3017597808

The FDA completed an inspection of Peter Gottlieb, MD on January 11, 2021 in Aurora, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 11, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Aurora, CO (United States)

Additional Details

Clinical Investigator (CI)