FDA Inspection 919565 - PureTek Corporation - March 18, 2015

FDA Inspection 919565 for PureTek Corporation on March 18, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 919565 for PureTek Corporation on March 18, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

PureTek Corporation

Inspection Date

March 18, 2015

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 27bb1542-f95e-475f-a0c6-00e3a54655d5

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