# Ulthera Inc – FDA Inspection, Nov 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/ulthera-inc/9ccc95d0-48db-4621-bd67-0ff2bb9e47c3
Source feed: FDA_Inspections

> FDA inspection 633629 of Ulthera Inc, November 24, 2009. Classification: Official Action Indicated (OAI). 10 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 633629
- Company Name: Ulthera Inc
- Inspection Date: 2009-11-24
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1290810 - 2025-10-28
- FDA Inspection 1209243 - 2023-06-22
- FDA Inspection 1103289 - 2019-09-18
- [FDA Inspection 1060604 - 2018-07-26](https://www.keypedia.com/records/fda_inspections/ulthera-inc/bf704cfb-cdfe-478b-b59c-bada010dcce2)
- FDA Inspection 1029899 - 2017-06-23

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