FDA Import Refusal FR1-0018903-9/41/1 — ASAHI POLYSLIDER CO.,LTD

ASAHI POLYSLIDER CO.,LTD — FEI 3012391968

The FDA refused shipment FR1-0018903-9/41/1 from ASAHI POLYSLIDER CO.,LTD (Japan) on Jan 22, 2024. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jan 22, 2024
Country
Japan
Product Category
Devices
Product Code
79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
Charges
118,508

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