FDA Import Refusal AEK-8239003-8/11/1 — SHENZHEN S HANDE TECHNOLOGY CO L

SHENZHEN S HANDE TECHNOLOGY CO L — FEI 3021316147

The FDA refused shipment AEK-8239003-8/11/1 from SHENZHEN S HANDE TECHNOLOGY CO L (China) on Feb 27, 2025. The refused product falls under Devices — ELECTROMAGNETIC STIMULATOR, PAIN RELIEF. Cited charges: 118,3280,333,508 This firm has 1 other import refusal on record.

Refusal Details

Date
Feb 27, 2025
Country
China
Product Category
Devices
Product Code
89QPL ELECTROMAGNETIC STIMULATOR, PAIN RELIEF
Charges
118,3280,333,508

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