FDA Inspection 1149608 — Yuki Gosei Kogyo Co., Ltd.

Yuki Gosei Kogyo Co., Ltd. — FEI 3002808534

The FDA completed an inspection of Yuki Gosei Kogyo Co., Ltd. on July 28, 2021 in Iwaki. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 28, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Iwaki (Japan)