FDA Import Refusal 799-9026776-6/11/1 — Abbott Rapid Diagnostics Jena GmbH
The FDA refused shipment 799-9026776-6/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Jul 7, 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
- Jul 7, 2022
- Country
- Germany
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 237,508