FDA Import Refusal AEK-9456357-1/12/1 — SHANDONG HUAMEI TECHNOLOGY CO.,LTD.

SHANDONG HUAMEI TECHNOLOGY CO.,LTD. — FEI 3016170453

The FDA refused shipment AEK-9456357-1/12/1 from SHANDONG HUAMEI TECHNOLOGY CO.,LTD. (China) on Aug 12, 2021. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Aug 12, 2021
Country
China
Product Category
Devices
Product Code
79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Charges
508

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