FDA Import Refusal AEK-7575642-7/10002/3 — Diomed Development

Diomed Development — FEI 3010120264

The FDA refused shipment AEK-7575642-7/10002/3 from Diomed Development (United Kingdom) on Aug 19, 2025. The refused product falls under Drugs and Biologics — SALICYLIC ACID (KERATOLYTIC). Cited charges: 118,3280

Refusal details

Date
Aug 19, 2025
Country
United Kingdom
Product Category
Drugs and Biologics
Product Code
64XBJ06 SALICYLIC ACID (KERATOLYTIC)
Charges
118,3280

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