FDA Import Refusal 799-4977268-3/11/1 — FUJIMORI KOGYO CO LTD
The FDA refused shipment 799-4977268-3/11/1 from FUJIMORI KOGYO CO LTD (Japan) on Jan 3, 2020. The refused product falls under Devices — AUTOMATED OCCULT BLOOD ANALYZER. Cited charges: 118,3280
Refusal details
- Date
- Jan 3, 2020
- Country
- Japan
- Product Category
- Devices
- Product Code
- 81OOX AUTOMATED OCCULT BLOOD ANALYZER
- Charges
- 118,3280