FDA Inspection 1243970 — EUROSIREL S.P.A

EUROSIREL S.P.A — FEI 3015892095

The FDA completed an inspection of EUROSIREL S.P.A on May 24, 2024 in Cusago. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cusago (Italy)