FDA Inspection 916050 — Robert A. Seder, MD

Robert A. Seder, MD — FEI 3011306882

The FDA completed an inspection of Robert A. Seder, MD on Feb 18, 2015 in Bethesda, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 18, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Bethesda, MD (United States)

Additional Details

Clinical Investigator (CI)