FDA Inspection 720696 - Zeltiq Aesthetics, Inc - April 19, 2011

FDA Inspection 720696 for Zeltiq Aesthetics, Inc on April 19, 2011. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 720696 for Zeltiq Aesthetics, Inc on April 19, 2011. Classification: No Action Indicated (NAI).

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Record Information

Company

Zeltiq Aesthetics, Inc

Inspection Date

April 19, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7088666-5eca-4310-842b-c1b9825a0a52

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