FDA Import Refusal AEK-0829508-0/100002/1 — TaiDoc Technology Corporation
The FDA refused shipment AEK-0829508-0/100002/1 from TaiDoc Technology Corporation (Taiwan) on Jul 24, 2026. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Jul 24, 2026
- Country
- Taiwan
- Product Category
- Devices
- Product Code
- 73CAF NEBULIZER (DIRECT PATIENT INTERFACE)
- Charges
- 341