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FDA Import Refusal FR1-0018722-3/11/1 — Goodman Co., Ltd

Goodman Co., Ltd — FEI 3007835716

The FDA refused shipment FR1-0018722-3/11/1 from Goodman Co., Ltd (Japan) on Jan 18, 2023. The refused product falls under Devices — CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE. Cited charge: 2780 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 18, 2023
Country
Japan
Product Category
Devices
Product Code
74LOX CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE
Charges
2780

Recent inspections

Other import refusals

FDA data resources

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