FDA Inspection 1286506 - Intertek USA Inc. - September 25, 2025

FDA Inspection 1286506 for Intertek USA Inc. on September 25, 2025. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1286506 for Intertek USA Inc. on September 25, 2025. Classification: No Action Indicated (NAI).

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Record Information

Company

Intertek USA Inc.

Inspection Date

September 25, 2025

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 7f342edb-ce60-471e-9a19-d9c6d57e4047

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