FDA Inspection 1035618 - Lonza AG - December 15, 2017

FDA Inspection 1035618 for Lonza AG on December 15, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1035618 for Lonza AG on December 15, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Lonza AG

Inspection Date

December 15, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: 6aabdbe9-cb78-4447-878b-509514b56a44

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