FDA Import Refusal 112-0448053-0/1/1 — Abilityone Kinetec Sa
The FDA refused shipment 112-0448053-0/1/1 from Abilityone Kinetec Sa (France) on Dec 11, 2007. The refused product falls under Devices — SPACER, CEMENT, ARTHROPLASTY, TOTAL JOINT. Cited charge: 118
Refusal details
- Date
- Dec 11, 2007
- Country
- France
- Product Category
- Devices
- Product Code
- 87NDX SPACER, CEMENT, ARTHROPLASTY, TOTAL JOINT
- Charges
- 118