FDA Inspection 981650 - Intertek USA Inc. - August 12, 2016

FDA Inspection 981650 for Intertek USA Inc. on August 12, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 981650 for Intertek USA Inc. on August 12, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Intertek USA Inc.

Inspection Date

August 12, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 55df2482-54f0-4339-9b35-8ddf9cc459fb

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