# Somnowell, Inc. – FDA Inspection, Mar 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/somnowell-inc/f7129059-637c-4303-85ea-a368ae075731
Source feed: FDA_Inspections

> FDA inspection 961419 of Somnowell, Inc., March 10, 2016. Classification: Official Action Indicated (OAI). 9 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961419
- Company Name: Somnowell, Inc.
- Inspection Date: 2016-03-10
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

Company: https://www.keypedia.com/companies/somnowell-inc/7f9ba2f6-b4db-4ab6-9d9f-c1314b1ececc

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