FDA Inspection 1220016 — Karen L. Kotloff, MD

Karen L. Kotloff, MD — FEI 3006004717

The FDA completed an inspection of Karen L. Kotloff, MD on September 15, 2023 in Baltimore, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 15, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Sponsor-Investigator (S-I)