FDA Import Refusal 799-0052110-4/11/1 — WEKO PHARMA
The FDA refused shipment 799-0052110-4/11/1 from WEKO PHARMA (Germany) on Feb 2, 2021. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charge: 508
Refusal details
- Date
- Feb 2, 2021
- Country
- Germany
- Product Category
- Devices
- Product Code
- 83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
- Charges
- 508