# FDA Inspection 663790 - Ulthera Inc - May 25, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/ulthera-inc/2e46779f-5102-4752-a30e-b45215c3f6a3
Source feed: FDA_Inspections

> FDA Inspection 663790 for Ulthera Inc on May 25, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 663790
- Company Name: Ulthera Inc
- Inspection Date: 2010-05-25
- Classification: No Action Indicated (NAI)
- 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/160c334b-0c06-432a-a7f8-a416c4b03314

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