FDA Import Refusal 508-0381976-7/101/8 — CORDIS DE MEXICO, SA DE CV

CORDIS DE MEXICO, SA DE CV — FEI 3003248396

The FDA refused shipment 508-0381976-7/101/8 from CORDIS DE MEXICO, SA DE CV (Mexico) on Jun 3, 2019. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charge: 118 This firm has 4 other import refusals on record.

Refusal Details

Date
Jun 3, 2019
Country
Mexico
Product Category
Devices
Product Code
74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
Charges
118

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