FDA Import Refusal AEK-2519756-5/11/1 — VIBRANT LTD

VIBRANT LTD — FEI 3014640407

The FDA refused shipment AEK-2519756-5/11/1 from VIBRANT LTD (Israel) on Jan 6, 2023. The refused product falls under Devices — DEVICE, INCONTINENCE, UROSHEATH TYPE. Cited charges: 118,3280,341 This firm has 1 other import refusal on record.

Refusal details

Date
Jan 6, 2023
Country
Israel
Product Category
Devices
Product Code
78EXJ DEVICE, INCONTINENCE, UROSHEATH TYPE
Charges
118,3280,341

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