# FDA Inspection 1301430 - Erika A. Petersen, M.D. - January 30, 2026

Source: https://www.keypedia.com/records/fda_inspections/erika-a-petersen-md/1e02a740-b1bb-40f4-acfd-dece249e45e7
Source feed: FDA_Inspections

> FDA Inspection 1301430 for Erika A. Petersen, M.D. on January 30, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1301430
- Company Name: Erika A. Petersen, M.D.
- Inspection Date: 2026-01-30
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1301430 - 2026-01-30](https://www.keypedia.com/records/fda_inspections/erika-a-petersen-md/0190a425-8ec1-408f-a357-0b8f2e3bee52)

Company: https://www.keypedia.com/companies/erika-a-petersen-md/571ed8c8-5604-4ff5-a2d1-e7854fb71188

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