FDA Import Refusal AEK-0935547-9/10002/1 — ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant
The FDA refused shipment AEK-0935547-9/10002/1 from ASAHI POLYSLIDER COMPANY, LIMITED Okayama-Kuse Plant (Japan) on Jul 14, 2026. The refused product falls under Devices — SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE. Cited charges: 118,3280,508
Refusal Details
- Date
- Jul 14, 2026
- Country
- Japan
- Product Category
- Devices
- Product Code
- 79FMK SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
- Charges
- 118,3280,508