FDA Import Refusal 231-8521078-3/31/5 — NIPRO CORP.
The FDA refused shipment 231-8521078-3/31/5 from NIPRO CORP. (Japan) on Oct 31, 2019. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charge: 479 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Oct 31, 2019
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
- Charges
- 479