# FDA Inspection 828792 - Zeltiq Aesthetics Inc. - April 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/zeltiq-aesthetics-inc/8cee3deb-bc9e-487d-a326-4637c8d2aa59
Source feed: FDA_Inspections

> FDA Inspection 828792 for Zeltiq Aesthetics Inc. on April 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 828792
- Company Name: Zeltiq Aesthetics Inc.
- Inspection Date: 2013-04-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 978938 - 2016-03-11](https://www.keypedia.com/records/fda_inspections/zeltiq-aesthetics-inc/e16ec21b-f282-4724-938f-4141691e531e)

Company: https://www.keypedia.com/companies/zeltiq-aesthetics-inc/706fb3cd-acb2-4570-9a8b-52408259ea02

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