FDA Import Refusal 799-4285614-6/11/1 — Abbott Rapid Diagnostics Jena GmbH

Abbott Rapid Diagnostics Jena GmbH — FEI 3016704892

The FDA refused shipment 799-4285614-6/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Aug 19, 2021. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 19, 2021
Country
Germany
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
508

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