FDA Import Refusal K51-0086647-1/21/1 — Luminex Corporation
The FDA refused shipment K51-0086647-1/21/1 from Luminex Corporation (United States) on November 9, 2016. The refused product falls under Devices — TEST, QUALITATIVE, FOR HLA, NON-DIAGNOSTIC. Cited charges: 3280,341
Refusal Details
- Date
- November 9, 2016
- Country
- United States
- Product Category
- Devices
- Product Code
- 81MZI TEST, QUALITATIVE, FOR HLA, NON-DIAGNOSTIC
- Charges
- 3280,341