Home / Import refusals / FR1-0017542-6/11/1

FDA Import Refusal FR1-0017542-6/11/1 — Goodman Co., Ltd

Goodman Co., Ltd — FEI 3007835716

The FDA refused shipment FR1-0017542-6/11/1 from Goodman Co., Ltd (Japan) on Mar 8, 2019. The refused product falls under Devices — CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Mar 8, 2019
Country
Japan
Product Category
Devices
Product Code
74LOX CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE
Charges
118

Recent inspections

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.