FDA Import Refusal 8DT-0007541-7/11/1 — Sysmex Corporation
The FDA refused shipment 8DT-0007541-7/11/1 from Sysmex Corporation (Japan) on Dec 23, 2022. The refused product falls under Devices — AUTOMATED OCCULT BLOOD ANALYZER. Cited charges: 118,341 This firm has 3 other import refusals on record.
Refusal Details
- Date
- Dec 23, 2022
- Country
- Japan
- Product Category
- Devices
- Product Code
- 81OOX AUTOMATED OCCULT BLOOD ANALYZER
- Charges
- 118,341