FDA Import Refusal AEK-4611068-8/11/1 — K-Axis Co., Ltd. (Japan)

K-Axis Co., Ltd. (Japan) — FEI 3030185508

The FDA refused shipment AEK-4611068-8/11/1 from K-Axis Co., Ltd. (Japan) (Japan) on Jan 24, 2024. The refused product falls under Radiological Health — GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL. Cited charge: 476

Refusal details

Date
Jan 24, 2024
Country
Japan
Product Category
Radiological Health
Product Code
95RDW GENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
Charges
476

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