FDA Import Refusal 799-0371232-0/11/1 — ABBOTT RAPID DIAGNOSTICS GERMANY

ABBOTT RAPID DIAGNOSTICS GERMANY — FEI 3016699023

The FDA refused shipment 799-0371232-0/11/1 from ABBOTT RAPID DIAGNOSTICS GERMANY (Germany) on Jan 8, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508

Refusal details

Date
Jan 8, 2021
Country
Germany
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508

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