FDA Inspection 893677 - Lonza AG - August 29, 2014

FDA Inspection 893677 for Lonza AG on August 29, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 893677 for Lonza AG on August 29, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza AG

Inspection Date

August 29, 2014

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: f16885c5-b179-45f7-b826-f1969e2e6fa9

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