FDA Import Refusal 799-7250833-5/11/1 — MOTION, INC
The FDA refused shipment 799-7250833-5/11/1 from MOTION, INC (South Korea) on Jun 15, 2020. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jun 15, 2020
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118,3280