FDA issued a Warning Letter to Yuki Gosei Kogyo Co., Ltd. on 7/17/2018 as a result of this inspection.
483 Yuki Gosei Kogyo Nov 2017

483 Yuki Gosei Kogyo Nov 2017

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FDA investigators audited the Yuki Gosei Kogyo - Iwaki, Japan facility and issued inspectional observations (via FDA 483) on 17 Nov 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 17 Nov 2017
  • Location: Iwaki, Japan
  • FEI: 3002808534
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