FDA Import Refusal 799-2515680-2/11/1 — Nipro Corporation
The FDA refused shipment 799-2515680-2/11/1 from Nipro Corporation (Japan) on Nov 18, 2019. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Nov 18, 2019
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 118