FDA Import Refusal AEK-9386168-7/11/1 — Abbott Rapid Diagnostics Jena GmbH

Abbott Rapid Diagnostics Jena GmbH — FEI 3016704892

The FDA refused shipment AEK-9386168-7/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Jul 16, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,237,3280,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 16, 2021
Country
Germany
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
118,237,3280,508

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