FDA Inspection 921050 — Robert Orenstein, DO

Robert Orenstein, DO — FEI 3011415995

The FDA completed an inspection of Robert Orenstein, DO on Apr 2, 2015 in Phoenix, AZ. 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 2, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance