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

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Record Details

This FDA Inspection record concerns Somnowell, Inc., with an inspection on March 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Somnowell, Inc.
Inspection Date: March 10, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · d7f3b9d2-2b3e-41d9-adfc-c8f019705868

Violation Codes9

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(i)21 CFR 820.30(j)21 CFR 820.4021 CFR 820.50

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