FDA Import Refusal 112-2576855-5/1/1 — Seirin Corporation
The FDA refused shipment 112-2576855-5/1/1 from Seirin Corporation (Japan) on Apr 12, 2004. The refused product falls under Devices — NEEDLE, ACUPUNCTURE, SINGLE USE. Cited charge: 118 This firm has 1 other import refusal on record.
Refusal Details
- Date
- Apr 12, 2004
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80MQX NEEDLE, ACUPUNCTURE, SINGLE USE
- Charges
- 118