FDA Import Refusal 9QB-0011555-2/30003/1 — AMPELMANN OPERATIONS BV

AMPELMANN OPERATIONS BV — FEI 3042304069

The FDA refused shipment 9QB-0011555-2/30003/1 from AMPELMANN OPERATIONS BV (Netherlands) on Jul 21, 2026. The refused product falls under Radiological Health — ALIGNMENT LASER PRODUCT, SURVEYING LEVELING, ALIGNMENT LASER PRODUCTS. Cited charge: 476

Refusal details

Date
Jul 21, 2026
Country
Netherlands
Product Category
Radiological Health
Product Code
95RER ALIGNMENT LASER PRODUCT, SURVEYING LEVELING, ALIGNMENT LASER PRODUCTS
Charges
476

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