FDA Inspection 1095974 — Astellas Pharma Inc.

Astellas Pharma Inc. — FEI 3002807003

The FDA completed an inspection of Astellas Pharma Inc. on May 31, 2019 in Toyama. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 31, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Toyama (Japan)

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