FDA Import Refusal 799-2897127-5/11/1 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA refused shipment 799-2897127-5/11/1 from NIPRO CORP. (Japan) on Aug 30, 2024. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Aug 30, 2024
Country
Japan
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3280,508

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.