FDA Import Refusal AEK-7767735-6/11/1 — MOTION, INC
The FDA refused shipment AEK-7767735-6/11/1 from MOTION, INC (South Korea) on Sep 1, 2020. The refused product falls under Devices — COVID-19 MULTI-ANALYTE RESPIRATORY PANEL NUCLEIC ACID DEVICES. Cited charge: 508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Sep 1, 2020
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 83QLT COVID-19 MULTI-ANALYTE RESPIRATORY PANEL NUCLEIC ACID DEVICES
- Charges
- 508