FDA Import Refusal 799-8615028-7/21/1 — Vitrex Medical A/S

Vitrex Medical A/S — FEI 3003208740

The FDA refused shipment 799-8615028-7/21/1 from Vitrex Medical A/S (Denmark) on January 11, 2017. 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.