FDA Inspection 1274304 — Astellas Pharma Inc.

Astellas Pharma Inc. — FEI 3002808523

The FDA completed an inspection of Astellas Pharma Inc. on Jun 6, 2025 in Takahagi. 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
Jun 6, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Takahagi (Japan)

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