FDA Import Refusal AX6-0001729-1/1/1 — Nihon Kohden Corp.
The FDA refused shipment AX6-0001729-1/1/1 from Nihon Kohden Corp. (Japan) on Apr 8, 2005. The refused product falls under Devices — DEFIBRILLATOR, AUTOMATIC, EXTERNAL, FOR OUT-OF-HOSPITAL USE. Cited charges: 341,508 This firm has 4 other import refusals on record.
Refusal details
- Date
- Apr 8, 2005
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74NPN DEFIBRILLATOR, AUTOMATIC, EXTERNAL, FOR OUT-OF-HOSPITAL USE
- Charges
- 341,508