FDA Import Refusal 799-8068714-6/11/1 — Roche Diabetes Care GmbH

Roche Diabetes Care GmbH — FEI 3011806823

The FDA refused shipment 799-8068714-6/11/1 from Roche Diabetes Care GmbH (Germany) on Nov 16, 2018. 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 5 or more other import refusals on record.

Refusal details

Date
Nov 16, 2018
Country
Germany
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,3280,508

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.