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FDA Import Refusal AEK-9696471-1/60002/1 — Prollenium Medical Technologies Inc.

Prollenium Medical Technologies Inc. — FEI 3004423487

The FDA refused shipment AEK-9696471-1/60002/1 from Prollenium Medical Technologies Inc. (Canada) on September 25, 2026. The refused product falls under Devices — IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE. Cited charges: 118,237,3280,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 25, 2026
Country
Canada
Product Category
Devices
Product Code
79LMH IMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
Charges
118,237,3280,75

Recent inspections

  • 1070919 (VAI Thu Nov 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1011040 (NAI Thu Apr 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

FDA data resources