FDA Import Refusal FR1-0011912-7/2/1 — Nipro Corporation
The FDA refused shipment FR1-0011912-7/2/1 from Nipro Corporation (Japan) on Aug 7, 2007. The refused product falls under Devices — NEEDLE, SPINAL, SHORT TERM. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Aug 7, 2007
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80MIA NEEDLE, SPINAL, SHORT TERM
- Charges
- 341