FDA Inspection 1223070 — Shionogi Pharma Co. Ltd.

Shionogi Pharma Co. Ltd. — FEI 3008353674

The FDA completed an inspection of Shionogi Pharma Co. Ltd. on Oct 20, 2023 in Tokushima. 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
Oct 20, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tokushima (Japan)

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