# FDA Inspection 738168 - Ulthera Inc - July 21, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/ulthera-inc/ff34939f-6374-4032-a1d0-769d252ec174/
Source feed: FDA_Inspections

> FDA Inspection 738168 for Ulthera Inc on July 21, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 738168
- Company Name: Ulthera Inc
- Inspection Date: 2011-07-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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