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FDA Import Refusal AEK-3538980-6/11/1 — LIFESCAN EUROPE GMBH

LIFESCAN EUROPE GMBH — FEI 3008382007

The FDA refused shipment AEK-3538980-6/11/1 from LIFESCAN EUROPE GMBH (Switzerland) on Aug 15, 2023. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280,508 This firm has 2 other import refusals on record.

Refusal Details

Date
Aug 15, 2023
Country
Switzerland
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,3280,508

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