FDA Inspection 1328216 — Sanofi S.R.L.

Sanofi S.R.L. — FEI 3002807108

The FDA completed an inspection of Sanofi S.R.L. on Oct 29, 2024 in Anagni. 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
Oct 29, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anagni (Italy)

Additional Details

Mutual Recognition Agreement (MRA)