FDA Inspection 1307162 — ANTEIS SA

ANTEIS SA — FEI 3015471896

The FDA completed an inspection of ANTEIS SA on February 27, 2026 in Lonay. 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
February 27, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Lonay (Switzerland)