# Ulthera Inc - Inspection Records

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

> Inspection records and compliance data for Ulthera Inc in Raleigh, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: Ulthera Inc
- FEI Number: 1012187
- City: Raleigh
- State: North Carolina
- Country Name: United States
- Address Line 1: 6501 Six Forks Rd
- Zip Code: 27615

## Related Documents

- [FDA Inspection 1290810 - Ulthera Inc - 2025-10-28](https://www.keypedia.com/records/fda_inspections/ulthera-inc/beb607d3-0471-4a4b-bdf1-3e63bf4b4717) — source: FDA, date: October 28, 2025
- [FDA Inspection 1290810 - Ulthera Inc - 2025-10-28](https://www.keypedia.com/records/fda_inspections/ulthera-inc/cda69a20-7f7a-429e-bfad-10a24ffba51e) — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2025
- [FDA Inspection 1209243 - Ulthera Inc - 2023-06-22](https://www.keypedia.com/records/fda_inspections/ulthera-inc/25907e91-8ffd-4c1d-8449-4b16b99e33a5) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2023
- [FDA Inspection 1103289 - Ulthera Inc - 2019-09-18](https://www.keypedia.com/records/fda_inspections/ulthera-inc/bb68c2d7-4bfb-4ba2-b581-c1aa007e2a8a) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2019
- [FDA Inspection 941155 - Ulthera Inc - 2015-08-07](https://www.keypedia.com/records/fda_inspections/ulthera-inc/f5fef2b5-fec4-4441-abf1-8bbda036482c) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2015
- [FDA Inspection 912381 - Ulthera Inc - 2015-01-26](https://www.keypedia.com/records/fda_inspections/ulthera-inc/08ea104f-b0bc-4763-9169-346f2a3ad99b) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2015
- [FDA Inspection 738168 - Ulthera Inc - 2011-07-21](https://www.keypedia.com/records/fda_inspections/ulthera-inc/ff34939f-6374-4032-a1d0-769d252ec174) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 21, 2011
- [FDA Inspection 738168 - Ulthera Inc - 2011-07-21](https://www.keypedia.com/records/fda_inspections/ulthera-inc/057af391-0859-4ad0-861f-9433b1e23f88) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2011
- [FDA Inspection 685618 - Ulthera Inc - 2010-09-29](https://www.keypedia.com/records/fda_inspections/ulthera-inc/b9ede10a-b487-4f9c-b127-07eeccc5b3e9) — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2010
- [FDA Inspection 641742 - Ulthera Inc - 2010-01-15](https://www.keypedia.com/records/fda_inspections/ulthera-inc/58c101a8-1a8b-495c-bb6b-1bec49917db4) — classification: No Action Indicated (NAI), source: FDA, date: January 15, 2010

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