FDA Import Refusal 799-1838114-7/11/1 — GLUCORX LTD

GLUCORX LTD — FEI 3021560564

The FDA refused shipment 799-1838114-7/11/1 from GLUCORX LTD (United Kingdom) on Jul 15, 2024. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charge: 118

Refusal Details

Date
Jul 15, 2024
Country
United Kingdom
Product Category
Devices
Product Code
80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
Charges
118

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