FDA Inspection 822364 - Fresenius USA, Inc. - February 22, 2013

FDA Inspection 822364 for Fresenius USA, Inc. on February 22, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 822364 for Fresenius USA, Inc. on February 22, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.30(g)

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Record Information

Company

Fresenius USA, Inc.

Inspection Date

February 22, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc5dcf43-7d33-4536-b14d-94fc71aa2ce4

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