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FDA Import Refusal AEK-9592353-6/10002/1C — Q-Med AB

Q-Med AB — FEI 3003347293

The FDA refused shipment AEK-9592353-6/10002/1C from Q-Med AB (Sweden) on September 16, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,3280,341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 16, 2026
Country
Sweden
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,237,3280,341

Recent inspections

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Other import refusals

FDA data resources