Akorn, Inc.November 10, 2009

FDA 483 - Akorn, Inc. - November 10, 2009

FDA 483 for Akorn, Inc. on November 10, 2009. Product: N/A. Access full analysis and detailed observations.

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Record Summary

FDA 483 for Akorn, Inc. on November 10, 2009. Product: N/A. Access full analysis and detailed observations.

Violation Codes

21 CFR 211

21 CFR 210

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Record Information

Company

Akorn, Inc.

Inspection Date

November 10, 2009

Product Type

Office

Chicago District Office

People

Debra I. Love (Investigator)

ID: f60cb2d9-b6f6-4c05-8afa-ee130626e106

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