FDA Inspection 1316810 — Vygon SA

Vygon SA — FEI 3009291251

The FDA completed an inspection of Vygon SA on March 19, 2026 in Ecouen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 19, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Ecouen (France)