FDA Import Refusal 112-8048479-5/5/2 — TERUMO CORPORATION
The FDA refused shipment 112-8048479-5/5/2 from TERUMO CORPORATION (Japan) on Aug 10, 2010. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 508 This firm has 3 other import refusals on record.
Refusal details
- Date
- Aug 10, 2010
- Country
- Japan
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 508