FDA Inspection 885212 — Cynthia E. Dunbar

Cynthia E. Dunbar — FEI 3010802820

The FDA completed an inspection of Cynthia E. Dunbar on Jun 25, 2014 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 25, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bethesda, MD (United States)

Additional Details

Clinical Investigator (CI)