FDA Import Refusal F23-4028624-4/10002/1 — BENELUX IMAGING B.V.

BENELUX IMAGING B.V. — FEI 3029521953

The FDA refused shipment F23-4028624-4/10002/1 from BENELUX IMAGING B.V. (Netherlands) on Apr 10, 2026. The refused product falls under Devices — SYSTEM, TOMOGRAPHY, COMPUTED, EMISSION. Cited charges: 118,3280 This firm has 1 other import refusal on record.

Refusal Details

Date
Apr 10, 2026
Country
Netherlands
Product Category
Devices
Product Code
90KPS SYSTEM, TOMOGRAPHY, COMPUTED, EMISSION
Charges
118,3280

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