Home / Import refusals / 799-5160425-3/11/1

FDA Import Refusal 799-5160425-3/11/1 — ARTHESYS

ARTHESYS — FEI 3012776242

The FDA refused shipment 799-5160425-3/11/1 from ARTHESYS (France) on Jan 21, 2020. The refused product falls under Devices — CATHETER, INTRAVASCULAR, SHORT TERM. Cited charges: 118,341,508 This firm has 2 other import refusals on record.

Refusal details

Date
Jan 21, 2020
Country
France
Product Category
Devices
Product Code
80FOZ CATHETER, INTRAVASCULAR, SHORT TERM
Charges
118,341,508

Other import refusals

FDA data resources

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