FDA Import Refusal 799-8339379-3/11/1 — Abbott Rapid Diagnostics Jena GmbH

Abbott Rapid Diagnostics Jena GmbH — FEI 3016704892

The FDA refused shipment 799-8339379-3/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Apr 28, 2022. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charges: 237,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 28, 2022
Country
Germany
Product Category
Devices
Product Code
83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
Charges
237,508

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