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FDA Import Refusal 799-7328621-5/11/1 — YORKTEST LABORATORIES LIMITED

YORKTEST LABORATORIES LIMITED — FEI 3003438526

The FDA refused shipment 799-7328621-5/11/1 from YORKTEST LABORATORIES LIMITED (United Kingdom) on May 9, 2025. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 508 This firm has 3 other import refusals on record.

Refusal Details

Date
May 9, 2025
Country
United Kingdom
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
508

Other import refusals

FDA data resources

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