FDA Import Refusal 799-7294899-5/11/1 — BTX INC

BTX INC — FEI 3021523056

The FDA refused shipment 799-7294899-5/11/1 from BTX INC (Canada) on Feb 9, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 237,508

Refusal details

Date
Feb 9, 2022
Country
Canada
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
237,508

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