# FDA Inspection 1295672 - Siesta Medical, Inc. - September 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/9d57b0a3-4edf-4227-9fbf-87b589d2cdcd
Source feed: FDA_Inspections

> FDA Inspection 1295672 for Siesta Medical, Inc. on September 30, 2025. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1295672
- Company Name: Siesta Medical, Inc.
- Inspection Date: 2025-09-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1295672 - 2025-09-30](https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/e5b61628-f5e6-4678-9227-196eda745ad4)
- [FDA Inspection 1295672 - 2025-09-30](https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/1388bd3c-c21d-4005-8f34-10bb8a2f5486)
- [FDA Inspection 1193401 - 2022-12-15](https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/e8e3fe26-8e0f-4674-b5e8-54ec40590032)
- [FDA Inspection 888058 - 2014-07-28](https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/ba7fee22-999d-4bde-8052-074e3f706dc4)
- [FDA Inspection 888058 - 2014-07-28](https://www.keypedia.com/records/fda_inspections/siesta-medical-inc/c7a69470-ba4d-433f-a63a-404c9e04baac)

Company: https://www.keypedia.com/companies/siesta-medical-inc/2193f4d6-5930-4a62-9a8e-d0ac137c2441

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