# FDA Inspection 955146 - Sientra, Inc - January 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/sientra-inc/51d1ef0e-270d-4b71-8665-e832bbc7710c
Source feed: FDA_Inspections

> FDA Inspection 955146 for Sientra, Inc on January 07, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 955146
- Company Name: Sientra, Inc
- Inspection Date: 2016-01-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 955146 - 2016-01-07](https://www.keypedia.com/records/fda_inspections/sientra-inc/7925af63-fd72-41c4-bf0a-6f6aa21eff70)
- [FDA Inspection 807414 - 2012-11-16](https://www.keypedia.com/records/fda_inspections/sientra-inc/a0991da5-7599-4a28-bb09-9d4fbfed1873)
- [FDA Inspection 595125 - 2009-07-07](https://www.keypedia.com/records/fda_inspections/sientra-inc/2868574b-5bda-4ce8-9631-f308a59359f6)

Company: https://www.keypedia.com/companies/sientra-inc/f40be978-98c8-4272-946d-10bf5a69184e

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