FDA Import Refusal 799-0859744-4/21/1 — GLOBAL HEADQUARTERS KYOTO

GLOBAL HEADQUARTERS KYOTO — FEI 3012670044

The FDA refused shipment 799-0859744-4/21/1 from GLOBAL HEADQUARTERS KYOTO (Japan) on Apr 12, 2019. The refused product falls under Devices — DETECTOR AND ALARM, ARRHYTHMIA. Cited charges: 118,3280,341

Refusal details

Date
Apr 12, 2019
Country
Japan
Product Category
Devices
Product Code
74DSI DETECTOR AND ALARM, ARRHYTHMIA
Charges
118,3280,341

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