FDA Inspection 806051 - Cutera, Inc. - November 05, 2012

FDA Inspection 806051 for Cutera, Inc. on November 05, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 806051 for Cutera, Inc. on November 05, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Cutera, Inc.

Inspection Date

November 5, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: e780ffde-39c1-4869-bdd2-6d99e417c67d

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