FDA Inspection 895043 — Shiseido Co., LTD

Shiseido Co., LTD — FEI 3001041089

The FDA completed an inspection of Shiseido Co., LTD on Aug 1, 2014 in Kakegawa. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 1, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kakegawa (Japan)

Citations

IDCFRDescription
189021 CFR 211.165(e)Test methods
430321 CFR 211.67(b)Written procedures fail to include
434321 CFR 211.160(b)(1)Incoming lots - conformance to written specs-

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