FDA Import Refusal 231-6038871-0/1/1 — KooJoo Trading Company
The FDA refused shipment 231-6038871-0/1/1 from KooJoo Trading Company (South Korea) on Oct 4, 2013. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 290 This firm has 1 other import refusal on record.
Refusal details
- Date
- Oct 4, 2013
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 290