FDA Inspection 953179 — Helena Rodbard, MD

Helena Rodbard, MD — FEI 3008281992

The FDA completed an inspection of Helena Rodbard, MD on Dec 15, 2015 in Rockville, 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
Dec 15, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Clinical Investigator (CI)