FDA Import Refusal 799-1384700-9/11/1 — Iqe (Europe) Ltd
The FDA refused shipment 799-1384700-9/11/1 from Iqe (Europe) Ltd (United Kingdom) on Mar 31, 2021. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Mar 31, 2021
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 508