FDA Import Refusal AEK-9696471-1/10002/1A — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA refused shipment AEK-9696471-1/10002/1A from Q-Med AB (Sweden) on September 25, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 218,237,3280,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 25, 2026
Country
Sweden
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
218,237,3280,75