FDA Inspection 1180433 — Eisai Manufacturing Limited

Eisai Manufacturing Limited — FEI 3008356774

The FDA completed an inspection of Eisai Manufacturing Limited on Jan 21, 2022 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
Jan 21, 2022
Fiscal Year
2022
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.