FDA Inspection 1285718 — Rebecca A. Kazin, MD

Rebecca A. Kazin, MD — FEI 3038623364

The FDA completed an inspection of Rebecca A. Kazin, MD on September 25, 2025 in North Bethesda, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
North Bethesda, MD (United States)

Additional Details

Clinical Investigator (CI)