FDA Inspection 1237510 — Eisai Inc.

Eisai Inc. — FEI 1000158705

The FDA completed an inspection of Eisai Inc. on Apr 9, 2024 in Baltimore, MD. 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
Apr 9, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baltimore, MD (United States)