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FDA Import Refusal 799-7706365-1/11/1 — CARDIMED ASIA MEDI

CARDIMED ASIA MEDI — FEI 3037736378

The FDA refused shipment 799-7706365-1/11/1 from CARDIMED ASIA MEDI (Turkey) on Jun 4, 2025. The refused product falls under Devices — CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE. Cited charges: 118,3280,341,508

Refusal Details

Date
Jun 4, 2025
Country
Turkey
Product Category
Devices
Product Code
74LOX CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE
Charges
118,3280,341,508

FDA data resources

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