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FDA Import Refusal AEK-4335667-1/11/1 — Roche Diagnostics GmbH

Roche Diagnostics GmbH — FEI 3002806559

The FDA refused shipment AEK-4335667-1/11/1 from Roche Diagnostics GmbH (Germany) on Mar 14, 2018. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,16 This firm has 5 or more other import refusals on record.

Refusal details

Date
Mar 14, 2018
Country
Germany
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,16

Recent inspections

Other import refusals

FDA data resources

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