FDA Inspection 1131429 — Gentium SRL

Gentium SRL — FEI 3003744181

The FDA completed an inspection of Gentium SRL on June 15, 2017 in Villa Guardia. 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
June 15, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Villa Guardia (Italy)

Additional Details

Mutual Recognition Agreement (MRA)