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

Source: https://www.globalkeysolutions.net/records/fda_inspections/zeltiq-aesthetics-inc/f7088666-5eca-4310-842b-c1b9825a0a52/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 720696
- Company Name: Zeltiq Aesthetics, Inc
- Inspection Date: 2011-04-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/zeltiq-aesthetics-inc/f1f18345-7ce6-4bfc-848f-2805030e6264

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7