FDA Import Refusal 799-7333533-3/11/1 — FLOWFLEX
The FDA refused shipment 799-7333533-3/11/1 from FLOWFLEX (United Kingdom) on Apr 8, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 2 other import refusals on record.
Refusal details
- Date
- Apr 8, 2022
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 508