FDA Import Refusal 799-4387775-2/11/1 — ABBOTT RAPID DIAGNOSTICS
The FDA refused shipment 799-4387775-2/11/1 from ABBOTT RAPID DIAGNOSTICS (United States) on Aug 16, 2021. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charge: 508 This firm has 2 other import refusals on record.
Refusal Details
- Date
- Aug 16, 2021
- Country
- United States
- Product Category
- Devices
- Product Code
- 83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
- Charges
- 508