FDA Import Refusal 799-2839382-7/11/1 — Median Diagnostics Inc

Median Diagnostics Inc — FEI 3010793281

The FDA refused shipment 799-2839382-7/11/1 from Median Diagnostics Inc (South Korea) on Sep 3, 2024. The refused product falls under Drugs and Biologics — BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.. Cited charge: 75

Refusal details

Date
Sep 3, 2024
Country
South Korea
Product Category
Drugs and Biologics
Product Code
57YH99 BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
Charges
75

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