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FDA Import Refusal 799-6335680-2/11/1 — LEADIX GMBH

LEADIX GMBH — FEI 3019907650

The FDA refused shipment 799-6335680-2/11/1 from LEADIX GMBH (Germany) on Apr 7, 2022. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508 This firm has 3 other import refusals on record.

Refusal Details

Date
Apr 7, 2022
Country
Germany
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508

Other import refusals

FDA data resources

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