FDA Inspection 738168 - Ulthera Inc - July 21, 2011

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

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Record Summary

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

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Record Information

Company

Ulthera Inc

Inspection Date

July 21, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff34939f-6374-4032-a1d0-769d252ec174

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