FDA Import Refusal FR1-0017720-8/11/1 — Goodman Co., Ltd
The FDA refused shipment FR1-0017720-8/11/1 from Goodman Co., Ltd (Japan) on Aug 15, 2019. The refused product falls under Devices — CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE. Cited charges: 118,2380,3280 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Aug 15, 2019
- Country
- Japan
- Product Category
- Devices
- Product Code
- 74LOX CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE
- Charges
- 118,2380,3280