FDA Inspection 1120121 — Eisai Manufacturing Limited

Eisai Manufacturing Limited — FEI 3008356774

The FDA completed an inspection of Eisai Manufacturing Limited on Nov 29, 2018 in Hatfield. 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
Nov 29, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hatfield (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)

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