# FDA Inspection 1290810 - Ulthera Inc - October 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/ulthera-inc/cda69a20-7f7a-429e-bfad-10a24ffba51e
Source feed: FDA_Inspections

> FDA Inspection 1290810 for Ulthera Inc on October 28, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290810
- Company Name: Ulthera Inc
- Inspection Date: 2025-10-28
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1290810 - 2025-10-28](https://www.keypedia.com/records/fda_inspections/ulthera-inc/beb607d3-0471-4a4b-bdf1-3e63bf4b4717)
- [FDA Inspection 1209243 - 2023-06-22](https://www.keypedia.com/records/fda_inspections/ulthera-inc/25907e91-8ffd-4c1d-8449-4b16b99e33a5)
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- [FDA Inspection 912381 - 2015-01-26](https://www.keypedia.com/records/fda_inspections/ulthera-inc/08ea104f-b0bc-4763-9169-346f2a3ad99b)

Company: https://www.keypedia.com/companies/ulthera-inc/5b496f74-108b-4d0a-9a6f-67ebc92ecda6

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