FDA Import Refusal 799-5366507-1/11/1 — GLOBAL ACCESS DIAGNOSTICS

GLOBAL ACCESS DIAGNOSTICS — FEI 3020589234

The FDA refused shipment 799-5366507-1/11/1 from GLOBAL ACCESS DIAGNOSTICS (United Kingdom) on Nov 5, 2021. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,237,3280,508

Refusal details

Date
Nov 5, 2021
Country
United Kingdom
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
118,237,3280,508

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