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FDA Import Refusal 799-1818115-7/11/2 — Vascutek, Ltd.

Vascutek, Ltd. — FEI 3002808437

The FDA refused shipment 799-1818115-7/11/2 from Vascutek, Ltd. (United Kingdom) on Nov 18, 2022. The refused product falls under Devices — PROSTHESIS, AORTIC VALVE, PERCUTANEOUSLY DELIVERED. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Nov 18, 2022
Country
United Kingdom
Product Category
Devices
Product Code
74NPT PROSTHESIS, AORTIC VALVE, PERCUTANEOUSLY DELIVERED
Charges
341

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Other import refusals

FDA data resources

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