FDA Inspection 1315544 — Seratec SAS

Seratec SAS — FEI 3003666337

The FDA completed an inspection of Seratec SAS on September 11, 2025 in Courville Sur Eure. 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
September 11, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Courville Sur Eure (France)

Additional Details

Mutual Recognition Agreement (MRA)