# FDA Inspection 1285718 - Rebecca A. Kazin, MD - September 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/rebecca-a-kazin-md/85f150b3-7995-4e7d-a5e2-35677e4ad57e
Source feed: FDA_Inspections

> FDA Inspection 1285718 for Rebecca A. Kazin, MD on September 25, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1285718
- Company Name: Rebecca A. Kazin, MD
- Inspection Date: 2025-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1285718 - 2025-09-25](https://www.keypedia.com/records/fda_inspections/rebecca-a-kazin-md/787ff879-0775-4736-8bce-f992c35712f3)

Company: https://www.keypedia.com/companies/rebecca-a-kazin-md/e4dda365-b912-4158-af0d-8f307ca29e0c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7