# FDA Inspection 641742 - Ulthera Inc - January 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/ulthera-inc/58c101a8-1a8b-495c-bb6b-1bec49917db4
Source feed: FDA_Inspections

> FDA Inspection 641742 for Ulthera Inc on January 15, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 641742
- Company Name: Ulthera Inc
- Inspection Date: 2010-01-15
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- 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