FDA Inspection 1135115 - Intertek USA Inc. - December 21, 2020

FDA Inspection 1135115 for Intertek USA Inc. on December 21, 2020. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1135115 for Intertek USA Inc. on December 21, 2020. Classification: No Action Indicated (NAI).

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Record Information

Company

Intertek USA Inc.

Inspection Date

December 21, 2020

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 2f48af36-ffc7-461e-9310-010d26e42ceb

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