FDA Inspection 816790 - Meiji Seika Pharma Co., Ltd. - December 14, 2012

FDA Inspection 816790 for Meiji Seika Pharma Co., Ltd. on December 14, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 816790 for Meiji Seika Pharma Co., Ltd. on December 14, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Meiji Seika Pharma Co., Ltd.

Inspection Date

December 14, 2012

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fe3a9e82-8328-4be0-ae84-84945660f594

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