FDA Import Refusal 799-0573801-7/11/1 — SKYLARK GROUPWIDE

SKYLARK GROUPWIDE — FEI 3014665206

The FDA refused shipment 799-0573801-7/11/1 from SKYLARK GROUPWIDE (Taiwan) on Mar 27, 2019. The refused product falls under Devices — MONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS). Cited charges: 118,341,508

Refusal details

Date
Mar 27, 2019
Country
Taiwan
Product Category
Devices
Product Code
74MWI MONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS)
Charges
118,341,508

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