FDA Import Refusal 799-0581956-0/11/1 — ROCHE REGISTRATION LTD
The FDA refused shipment 799-0581956-0/11/1 from ROCHE REGISTRATION LTD (United Kingdom) on Jan 20, 2021. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charge: 508
Refusal details
- Date
- Jan 20, 2021
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
- Charges
- 508