FDA Inspection 1020783 - Handylee Enterprises (USA) Corp. - August 07, 2017

FDA Inspection 1020783 for Handylee Enterprises (USA) Corp. on August 07, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1020783 for Handylee Enterprises (USA) Corp. on August 07, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 1.502(a)

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Record Information

Company

Handylee Enterprises (USA) Corp.

Inspection Date

August 7, 2017

Product Type

Food/Cosmetics

ID: fe9f25e1-95ea-4343-8baa-6c015ba7998c

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