FDA Import Refusal AEK-8733785-0/41/1 — LUNGENE RAPID TEST

LUNGENE RAPID TEST — FEI 3017928625

The FDA refused shipment AEK-8733785-0/41/1 from LUNGENE RAPID TEST (Germany) on Feb 18, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508

Refusal details

Date
Feb 18, 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.