FDA Import Refusal AEK-0341022-0/12/1 — Shenzhen Urion Technology Co Ltd
The FDA refused shipment AEK-0341022-0/12/1 from Shenzhen Urion Technology Co Ltd (China) on Mar 10, 2022. The refused product falls under Devices — SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Mar 10, 2022
- Country
- China
- Product Category
- Devices
- Product Code
- 74DXN SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
- Charges
- 118,3280