FDA Inspection 1017463 — Tateyama Kasei Company Ltd.

Tateyama Kasei Company Ltd. — FEI 3003973547

The FDA completed an inspection of Tateyama Kasei Company Ltd. on July 5, 2017 in Imizu. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 5, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Imizu (Japan)

Citations

IDCFRDescription
121 CFR 11Electronic records