FDA Inspection 967811 - Lonza AG - March 11, 2016

FDA Inspection 967811 for Lonza AG on March 11, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 967811 for Lonza AG on March 11, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza AG

Inspection Date

March 11, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: d3cf442a-abb3-4302-8fda-dc73abdabba3

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