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FDA Import Refusal SCS-8766623-7/11/1 — Djo Canada

Djo Canada — FEI 3008261413

The FDA refused shipment SCS-8766623-7/11/1 from Djo Canada (Canada) on Mar 6, 2020. The refused product falls under Devices — CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE. Cited charges: 118,3280,508

Refusal details

Date
Mar 6, 2020
Country
Canada
Product Category
Devices
Product Code
74LOX CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS & OPERATIVE
Charges
118,3280,508

FDA data resources

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