FDA Inspection 1182037 — Sanofi S.R.L.

Sanofi S.R.L. — FEI 3006947840

The FDA completed an inspection of Sanofi S.R.L. on May 20, 2022 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
May 20, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Scoppito (Italy)

Additional Details

Mutual Recognition Agreement (MRA)