FDA Import Refusal 799-0678241-3/11/1 — IPPO JAPAN COMPANY

IPPO JAPAN COMPANY — FEI 3030668920

The FDA refused shipment 799-0678241-3/11/1 from IPPO JAPAN COMPANY (Japan) on Jun 6, 2024. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,3280

Refusal Details

Date
Jun 6, 2024
Country
Japan
Product Category
Devices
Product Code
80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
Charges
118,3280

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