FDA Import Refusal AEK-0700754-4/10002/1 — Citieffe Srl
The FDA refused shipment AEK-0700754-4/10002/1 from Citieffe Srl (Italy) on July 7, 2026. The refused product falls under Devices — ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES. Cited charges: 118,476
Refusal Details
- Date
- July 7, 2026
- Country
- Italy
- Product Category
- Devices
- Product Code
- 87HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
- Charges
- 118,476