FDA Inspection 1030478 - Catalent Indiana, LLC - May 19, 2017

FDA Inspection 1030478 for Catalent Indiana, LLC on May 19, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1030478 for Catalent Indiana, LLC on May 19, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Catalent Indiana, LLC

Inspection Date

May 19, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 8bcaeb7f-53f7-4eae-8c26-a1ffe037141a

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