FDA Import Refusal 799-7156936-2/11/1 — Johnson & Johnson

Johnson & Johnson — FEI 3005134259

The FDA refused shipment 799-7156936-2/11/1 from Johnson & Johnson (Canada) on Feb 22, 2022. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 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
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508

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