FDA Inspection 950673 - Akorn, Inc. - December 18, 2015

FDA Inspection 950673 for Akorn, Inc. on December 18, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 950673 for Akorn, Inc. on December 18, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Akorn, Inc.

Inspection Date

December 18, 2015

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fbf3f256-7811-4dcc-8f07-3424b0d25ac7

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