FDA Import Refusal 799-2434462-7/10003/1 — JIANGSU KERSEN MEDICAL INSTRUMENT CO., LTD.

JIANGSU KERSEN MEDICAL INSTRUMENT CO., LTD. — FEI 3010375033

The FDA refused shipment 799-2434462-7/10003/1 from JIANGSU KERSEN MEDICAL INSTRUMENT CO., LTD. (China) on Oct 14, 2025. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,341,508 This firm has 1 other import refusal on record.

Refusal Details

Date
Oct 14, 2025
Country
China
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,341,508

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