FDA Inspection 1034470 — Eisai Co., Ltd.

Eisai Co., Ltd. — FEI 3002806886

The FDA completed an inspection of Eisai Co., Ltd. on Sep 15, 2017 in Kamisu. 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). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kamisu (Japan)

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