FDA Import Refusal AEK-0102068-2/11/1 — SYNECTIV LTD

SYNECTIV LTD — FEI 3020886640

The FDA refused shipment AEK-0102068-2/11/1 from SYNECTIV LTD (United Kingdom) on Dec 13, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,341

Refusal details

Date
Dec 13, 2021
Country
United Kingdom
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
118,341

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