FDA Import Refusal AEK-8906335-5/11/1 — Roche Diagnostics

Roche Diagnostics — FEI 3004764267

The FDA refused shipment AEK-8906335-5/11/1 from Roche Diagnostics (France) on Mar 31, 2021. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Mar 31, 2021
Country
France
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
508

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