# FDA Inspection 633629 - Ulthera Inc - November 24, 2009

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

> FDA Inspection 633629 for Ulthera Inc on November 24, 2009. Classification: Official Action Indicated (OAI).

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## Details

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

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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