FDA Inspection 754208 - ThyssenKrupp Access Manufacturing, LLC - November 10, 2011

FDA Inspection 754208 for ThyssenKrupp Access Manufacturing, LLC on November 10, 2011. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 754208 for ThyssenKrupp Access Manufacturing, LLC on November 10, 2011. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(c)

21 CFR 820.22

21 CFR 820.250(a)

21 CFR 820.50

21 CFR 820.50(a)(1)

21 CFR 820.80(b)

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Record Information

Company

ThyssenKrupp Access Manufacturing, LLC

Inspection Date

November 10, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8de10fa-c121-45e2-bce1-1836939f7b6c

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