FDA Import Refusal AEK-2056482-8/20002/1 — TaiDoc Technology Corporation
The FDA refused shipment AEK-2056482-8/20002/1 from TaiDoc Technology Corporation (Taiwan) on Sep 18, 2026. The refused product falls under Devices — MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY. Cited charge: 3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Sep 18, 2026
- Country
- Taiwan
- Product Category
- Devices
- Product Code
- 79QRL MULTIPLE USE BLOOD LANCET FOR SINGLE PATIENT USE ONLY
- Charges
- 3280