FDA Inspection 983892 - Cutera, Inc. - August 19, 2016

FDA Inspection 983892 for Cutera, Inc. on August 19, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 983892 for Cutera, Inc. on August 19, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Cutera, Inc.

Inspection Date

August 19, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 7e19638e-f37c-4dfb-8d73-a073cdb9026a

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