FDA Import Refusal 267-0128049-2/1/1 — Kinetec Abilityone S.A.
The FDA refused shipment 267-0128049-2/1/1 from Kinetec Abilityone S.A. (France) on Mar 14, 2014. The refused product falls under Devices — EXERCISER, POWERED. Cited charge: 508
Refusal details
- Date
- Mar 14, 2014
- Country
- France
- Product Category
- Devices
- Product Code
- 89BXB EXERCISER, POWERED
- Charges
- 508