FDA Import Refusal AEK-0407387-8/11/1 — Abbott Rapid Diagnostics Jena GmbH
The FDA refused shipment AEK-0407387-8/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Feb 16, 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 16, 2022
- Country
- Germany
- Product Category
- Devices
- Product Code
- 83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
- Charges
- 508