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FDA Import Refusal AEK-5283179-6/11/1 — VIBRANT LTD

VIBRANT LTD — FEI 3014640407

The FDA refused shipment AEK-5283179-6/11/1 from VIBRANT LTD (Israel) on Nov 9, 2018. The refused product falls under Devices — GASTROINTESTINAL MOTILITY SYSTEM, CAPSULE. Cited charge: 3081 This firm has 1 other import refusal on record.

Refusal details

Date
Nov 9, 2018
Country
Israel
Product Category
Devices
Product Code
78NYV GASTROINTESTINAL MOTILITY SYSTEM, CAPSULE
Charges
3081

Other import refusals

FDA data resources

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