FDA Inspection 1263062 - Intertek USA Inc. - March 07, 2025

FDA Inspection 1263062 for Intertek USA Inc. on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1263062 for Intertek USA Inc. on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 11

21 CFR 211.22(d)

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Record Information

Company

Intertek USA Inc.

Inspection Date

March 7, 2025

Product Type

Biologics

Office

Center for Biologics Evaluation and Research

ID: 67862125-798a-4c6f-8bc7-690616177084

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