FDA Inspection 1010010 — David S. Rosenberg, MD

David S. Rosenberg, MD — FEI 3013100134

The FDA completed an inspection of David S. Rosenberg, MD on April 21, 2017 in Florissant, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Florissant, MO (United States)

Additional Details

Clinical Investigator (CI)