FDA Import Refusal 799-1709202-3/11/1 — Kyocera
The FDA refused shipment 799-1709202-3/11/1 from Kyocera (Japan) on May 30, 2019. The refused product falls under Devices — PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER. Cited charge: 118
Refusal details
- Date
- May 30, 2019
- Country
- Japan
- Product Category
- Devices
- Product Code
- 87KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER
- Charges
- 118