FDA Inspection 988050 - Yuki Gosei Kogyo Co., Ltd. - September 02, 2016

FDA Inspection 988050 for Yuki Gosei Kogyo Co., Ltd. on September 02, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 988050 for Yuki Gosei Kogyo Co., Ltd. on September 02, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Yuki Gosei Kogyo Co., Ltd.

Inspection Date

September 2, 2016

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: fca11665-6b9d-46b7-adbd-526b2f6e3f06

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