FDA Import Refusal 799-1384712-4/11/1 — IQE EUROPE LTD
The FDA refused shipment 799-1384712-4/11/1 from IQE EUROPE LTD (United Kingdom) on Mar 15, 2021. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508
Refusal details
- Date
- Mar 15, 2021
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 508