FDA Inspection 860979 - PureTek Corporation - December 18, 2013

FDA Inspection 860979 for PureTek Corporation on December 18, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 860979 for PureTek Corporation on December 18, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

PureTek Corporation

Inspection Date

December 18, 2013

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: a8442159-0b2b-4cf1-ae07-ab0234cddc91

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