FDA Inspection 940787 - Lonza Manufacturing LLC - August 28, 2015

FDA Inspection 940787 for Lonza Manufacturing LLC on August 28, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 940787 for Lonza Manufacturing LLC on August 28, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza Manufacturing LLC

Inspection Date

August 28, 2015

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 641ceb84-a9aa-4928-a80e-85c7461f969d

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