FDA Inspection 808852 - Reumofan USA LLC - December 03, 2012

FDA Inspection 808852 for Reumofan USA LLC on December 03, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 808852 for Reumofan USA LLC on December 03, 2012. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 111.453

21 CFR 111.455(a)

21 CFR 111.475(b)(2)

21 CFR 111.553

21 CFR 111.560(a)(1)

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Record Information

Company

Reumofan USA LLC

Inspection Date

December 3, 2012

Product Type

Food/Cosmetics

ID: f990a8b8-7be6-4ea9-9983-dbbd6d25dee6

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