FDA Inspection 1023175 - Daiwa Pharmaceutical Co., Ltd. - July 21, 2017

FDA Inspection 1023175 for Daiwa Pharmaceutical Co., Ltd. on July 21, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1023175 for Daiwa Pharmaceutical Co., Ltd. on July 21, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Daiwa Pharmaceutical Co., Ltd.

Inspection Date

July 21, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fe19a16c-28f7-47f9-a384-5a003cc060b1

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