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FDA Import Refusal 799-4441273-1/11/1 — ARTHESYS

ARTHESYS — FEI 3012776242

The FDA refused shipment 799-4441273-1/11/1 from ARTHESYS (France) on Dec 2, 2019. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charges: 118,3280,341,508 This firm has 2 other import refusals on record.

Refusal details

Date
Dec 2, 2019
Country
France
Product Category
Devices
Product Code
74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
Charges
118,3280,341,508

Other import refusals

FDA data resources

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