FDA Inspection 985197 - BioSerenity USA, Inc. - September 06, 2016

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Record Details

This FDA Inspection record concerns BioSerenity USA, Inc., with an inspection on September 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: BioSerenity USA, Inc.
Inspection Date: September 6, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1ec645e4-2269-4e9b-8ece-484746b1f0bb

Violation Codes2

21 CFR 820.2221 CFR 820.250(a)

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