FDA Inspection 846043 - Lonza Guangzhou Pharmaceutical Ltd. - August 23, 2013

FDA Inspection 846043 for Lonza Guangzhou Pharmaceutical Ltd. on August 23, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 846043 for Lonza Guangzhou Pharmaceutical Ltd. on August 23, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza Guangzhou Pharmaceutical Ltd.

Inspection Date

August 23, 2013

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 6173e794-a20c-4232-b5fe-2d603c6d7df3

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