FDA Inspection 1293450 — Sucampo Pharma, LLC

Sucampo Pharma, LLC — FEI 3004520523

The FDA completed an inspection of Sucampo Pharma, LLC on Nov 7, 2025 in Sanda. 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
Nov 7, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sanda (Japan)

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