FDA Import Refusal 799-8194251-9/11/1 — COVIDIEN JAPAN

COVIDIEN JAPAN — FEI 3012418485

The FDA refused shipment 799-8194251-9/11/1 from COVIDIEN JAPAN (Japan) on Jan 18, 2024. The refused product falls under Devices — ELECTROSURGICAL, CUTTING & COAGULATION, ACCESSORIES LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED. Cited charge: 118 This firm has 4 other import refusals on record.

Refusal Details

Date
Jan 18, 2024
Country
Japan
Product Category
Devices
Product Code
79NUJ ELECTROSURGICAL, CUTTING & COAGULATION, ACCESSORIES LAPAROSCOPIC & ENDOSCOPIC, REPROCESSED
Charges
118

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