FDA Import Refusal AEK-0844781-4/10002/1 — Zhejiang Gongdong Medical Technology Co., Ltd

Zhejiang Gongdong Medical Technology Co., Ltd — FEI 3005739529

The FDA refused shipment AEK-0844781-4/10002/1 from Zhejiang Gongdong Medical Technology Co., Ltd (China) on Jul 16, 2026. The refused product falls under Devices — MIXER, BLOOD TUBE. Cited charges: 118,341 This firm has 1 other import refusal on record.

Refusal Details

Date
Jul 16, 2026
Country
China
Product Category
Devices
Product Code
75GLE MIXER, BLOOD TUBE
Charges
118,341

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.