FDA Inspection 615025 - Lonza Manufacturing LLC - September 28, 2009

FDA Inspection 615025 for Lonza Manufacturing LLC on September 28, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 615025 for Lonza Manufacturing LLC on September 28, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza Manufacturing LLC

Inspection Date

September 28, 2009

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: c75b736f-20c2-4aa1-9ffe-9bdaedb1b275

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