FDA Import Refusal AEK-9425396-8/10002/1 — Aktiia SA

Aktiia SA — FEI 3019575688

The FDA refused shipment AEK-9425396-8/10002/1 from Aktiia SA (Switzerland) on February 19, 2026. The refused product falls under Devices — SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE. Cited charges: 118,3280,508 This firm has 1 other import refusal on record.