FDA Import Refusal AEK-1358903-9/11/1 — Taichi Holdings Limited
The FDA refused shipment AEK-1358903-9/11/1 from Taichi Holdings Limited (Japan) on Jul 26, 2022. The refused product falls under Devices — REPROCESSED INTRAVASCULAR ULTRASOUND CATHETER. Cited charges: 118,3280,341,508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jul 26, 2022
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74OWQ REPROCESSED INTRAVASCULAR ULTRASOUND CATHETER
- Charges
- 118,3280,341,508