FDA Import Refusal AEK-5229248-7/11/1 — Trillium MediVision Inc.
The FDA refused shipment AEK-5229248-7/11/1 from Trillium MediVision Inc. (Canada) on Jun 3, 2024. The refused product falls under Devices — LENS, INTRAOCULAR. Cited charges: 118,3280,341
Refusal Details
- Date
- Jun 3, 2024
- Country
- Canada
- Product Category
- Devices
- Product Code
- 86HQL LENS, INTRAOCULAR
- Charges
- 118,3280,341