# FDA Inspection 961419 - Somnowell, Inc. - March 10, 2016

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

> FDA Inspection 961419 for Somnowell, Inc. on March 10, 2016. Classification: Official Action Indicated (OAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 961419 - 2016-03-10](https://www.globalkeysolutions.net/api/records/fda_inspections/somnowell-inc/d7f3b9d2-2b3e-41d9-adfc-c8f019705868/)

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

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