FDA Inspection 1331820 — Sanofi S.R.L.

Sanofi S.R.L. — FEI 3006947840

The FDA completed an inspection of Sanofi S.R.L. on Dec 13, 2024 in Scoppito. 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
Dec 13, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Scoppito (Italy)

Additional Details

Mutual Recognition Agreement (MRA)