FDA Inspection 647477 - Intertek USA Inc. - March 03, 2010

FDA Inspection 647477 for Intertek USA Inc. on March 03, 2010. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 647477 for Intertek USA Inc. on March 03, 2010. Classification: No Action Indicated (NAI).

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Record Information

Company

Intertek USA Inc.

Inspection Date

March 3, 2010

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 0d58826a-4b3a-4030-91f5-a3b87b4613e1

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