FDA Import Refusal AEK-8611858-3/10002/1 — Laytec In-Line Gmbh

Laytec In-Line Gmbh — FEI 3009043595

The FDA refused shipment AEK-8611858-3/10002/1 from Laytec In-Line Gmbh (Germany) on Nov 26, 2025. The refused product falls under Radiological Health — GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL. Cited charges: 333,47,476

Refusal details

Date
Nov 26, 2025
Country
Germany
Product Category
Radiological Health
Product Code
95RDW GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
Charges
333,47,476

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