FDA Import Refusal BDN-0192448-4/31/1 — Hansol Medical

Hansol Medical — FEI 3005417950

The FDA refused shipment BDN-0192448-4/31/1 from Hansol Medical (South Korea) on Feb 6, 2024. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Feb 6, 2024
Country
South Korea
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,508

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