FDA Import Refusal FR1-0016944-5/31/1 — ASAHI POLYSLIDER CO.,LTD

ASAHI POLYSLIDER CO.,LTD — FEI 3012391968

The FDA refused shipment FR1-0016944-5/31/1 from ASAHI POLYSLIDER CO.,LTD (Japan) on Jun 12, 2017. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 12, 2017
Country
Japan
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118

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