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FDA Import Refusal 799-7171917-3/11/1 — BTNX Inc.

BTNX Inc. — FEI 3003917514

The FDA refused shipment 799-7171917-3/11/1 from BTNX Inc. (Canada) on Feb 22, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 237,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Feb 22, 2022
Country
Canada
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
237,508

Other import refusals

FDA data resources

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