FDA Inspection 835548 — Raphaela Goldbach-Mansky, MD

Raphaela Goldbach-Mansky, MD — FEI 3010179497

The FDA completed an inspection of Raphaela Goldbach-Mansky, MD on Jun 12, 2013 in Bethesda, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 12, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bethesda, MD (United States)

Additional Details

Clinical Investigator (CI)