FDA Import Refusal 1FX-3972655-0/10002/1 — Seirin Corporation
The FDA refused shipment 1FX-3972655-0/10002/1 from Seirin Corporation (Japan) on Sep 28, 2026. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charges: 118,3280,3904,3905 This firm has 1 other import refusal on record.
Refusal Details
- Date
- Sep 28, 2026
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
- Charges
- 118,3280,3904,3905