FDA Import Refusal AEK-0899170-4/10002/1 — ANTEIS SA

ANTEIS SA — FEI 3012201144

The FDA refused shipment AEK-0899170-4/10002/1 from ANTEIS SA (Switzerland) on Jul 24, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Jul 24, 2026
Country
Switzerland
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,3280

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