FDA Inspection 1034952 - PureTek Corporation - December 15, 2017

FDA Inspection 1034952 for PureTek Corporation on December 15, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1034952 for PureTek Corporation on December 15, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.67(a)

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Record Information

Company

PureTek Corporation

Inspection Date

December 15, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 8f390d5c-07c0-4bc1-adcf-f3590025d6cf

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