FDA Import Refusal ADK-1712342-2/2/1 — Koyo Business Service Inc
The FDA refused shipment ADK-1712342-2/2/1 from Koyo Business Service Inc (Japan) on May 13, 2009. The refused product falls under Devices — GLOVE, PATIENT EXAMINATION, LATEX. Cited charge: 118
Refusal details
- Date
- May 13, 2009
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80LYY GLOVE, PATIENT EXAMINATION, LATEX
- Charges
- 118