FDA Import Refusal AEK-0291086-5/11/1 — WOUNDCHEK LABORATORIES

WOUNDCHEK LABORATORIES — FEI 3021153641

The FDA refused shipment AEK-0291086-5/11/1 from WOUNDCHEK LABORATORIES (United Kingdom) on Jan 10, 2022. The refused product falls under Devices — ASSAY FOR DETECTION OF INFECTION IN CHRONIC WOUNDS. Cited charges: 118,3280,508

Refusal details

Date
Jan 10, 2022
Country
United Kingdom
Product Category
Devices
Product Code
83QFA ASSAY FOR DETECTION OF INFECTION IN CHRONIC WOUNDS
Charges
118,3280,508

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