FDA Import Refusal 799-8112115-2/11/1 — ACCUVEIN INC
The FDA refused shipment 799-8112115-2/11/1 from ACCUVEIN INC (United States) on Nov 16, 2018. The refused product falls under Devices — DEVICE, VEIN LOCATION, LIQUID CRYSTAL. Cited charges: 3280,341
Refusal Details
- Date
- Nov 16, 2018
- Country
- United States
- Product Category
- Devices
- Product Code
- 80KZA DEVICE, VEIN LOCATION, LIQUID CRYSTAL
- Charges
- 3280,341