FDA Inspection 633707 - BioSerenity USA, Inc. - January 05, 2010

FDA Inspection 633707 for BioSerenity USA, Inc. on January 05, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 633707 for BioSerenity USA, Inc. on January 05, 2010. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)(1)

21 CFR 820.25(b)

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Record Information

Company

BioSerenity USA, Inc.

Inspection Date

January 5, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa80b4b7-0d71-4893-b425-fa314768261b

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