FDA Import Refusal AEK-7122436-1/11/1 — Surescreen Diagnostics Limited

Surescreen Diagnostics Limited — FEI 3003082744

The FDA refused shipment AEK-7122436-1/11/1 from Surescreen Diagnostics Limited (United Kingdom) on May 18, 2020. The refused product falls under Devices — REAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
May 18, 2020
Country
United Kingdom
Product Category
Devices
Product Code
83QJR REAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID
Charges
508

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