# FDA Inspection 1286174 - Rebecca Hartman, M.D., M.P.H. - October 01, 2025

Source: https://www.keypedia.com/records/fda_inspections/rebecca-hartman-md-mph/e64d3c35-41c3-477a-ba60-57cccae5ef9f
Source feed: FDA_Inspections

> FDA Inspection 1286174 for Rebecca Hartman, M.D., M.P.H. on October 01, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1286174
- Company Name: Rebecca Hartman, M.D., M.P.H.
- Inspection Date: 2025-10-01
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1286174 - 2025-10-01](https://www.keypedia.com/records/fda_inspections/rebecca-hartman-md-mph/a8b97156-f2b0-4c96-ae56-f585b97841d3)

Company: https://www.keypedia.com/companies/rebecca-hartman-md-mph/bfc4c328-ccdc-4fa2-9634-5c5989d92c2c

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