FDA Inspection 815726 - Intertek USA Inc. - January 21, 2013

FDA Inspection 815726 for Intertek USA Inc. on January 21, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 815726 for Intertek USA Inc. on January 21, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Intertek USA Inc.

Inspection Date

January 21, 2013

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: e7a3457b-9987-41b5-8ccb-28b5d0db710b

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