FDA Import Refusal AEK-8435140-0/11/1 — AKTIIA BV
The FDA refused shipment AEK-8435140-0/11/1 from AKTIIA BV (Netherlands) on April 15, 2025. 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.
Refusal Details
- Date
- April 15, 2025
- Country
- Netherlands
- Product Category
- Devices
- Product Code
- 74DXN SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
- Charges
- 118,3280,508