FDA Inspection 1262436 - PureTek Corporation - March 07, 2025

FDA Inspection 1262436 for PureTek Corporation on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1262436 for PureTek Corporation on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 211.122(d)

21 CFR 211.25(a)

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Record Information

Company

PureTek Corporation

Inspection Date

March 7, 2025

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 382ace29-ecb5-4d12-a328-dbc5f752070a

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