FDA Import Refusal FR1-0018248-9/71/1 — ASAHI POLYSLIDER CO.,LTD
The FDA refused shipment FR1-0018248-9/71/1 from ASAHI POLYSLIDER CO.,LTD (Japan) on Jan 11, 2022. 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
- Jan 11, 2022
- Country
- Japan
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118