FDA Inspection 1037750 — Yuki Gosei Kogyo Co., Ltd.

Yuki Gosei Kogyo Co., Ltd. — FEI 3002808534

The FDA completed an inspection of Yuki Gosei Kogyo Co., Ltd. on Nov 17, 2017 in Iwaki. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Nov 17, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Iwaki (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.