FDA Import Refusal 799-8609961-1/11/1 — Aurora Biomed, Inc.

Aurora Biomed, Inc. — FEI 3004098682

The FDA refused shipment 799-8609961-1/11/1 from Aurora Biomed, Inc. (Canada) on Apr 21, 2022. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charges: 237,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Apr 21, 2022
Country
Canada
Product Category
Devices
Product Code
83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
Charges
237,508

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