FDA Inspection 996385 — Sucampo Pharma, LLC

Sucampo Pharma, LLC — FEI 3004520523

The FDA completed an inspection of Sucampo Pharma, LLC on November 11, 2016 in Sanda. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 11, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sanda (Japan)