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