FDA Import Refusal 112-8969310-6/1/1E — Nipro Medical Industries Ltd
The FDA refused shipment 112-8969310-6/1/1E from Nipro Medical Industries Ltd (Japan) on Jul 25, 2011. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Jul 25, 2011
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80NKK NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED
- Charges
- 118