Home / Import refusals / AEK-0844781-4/30003/1

FDA Import Refusal AEK-0844781-4/30003/1 — Zhejiang Gongdong Medical Technology Co., Ltd

Zhejiang Gongdong Medical Technology Co., Ltd — FEI 3005739529

The FDA refused shipment AEK-0844781-4/30003/1 from Zhejiang Gongdong Medical Technology Co., Ltd (China) on Jul 16, 2026. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. 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
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,341

Recent inspections

Other import refusals

FDA data resources

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