FDA Import Refusal AEK-2073256-3/2/1 — Prostrap Takeda Uk Limited
The FDA refused shipment AEK-2073256-3/2/1 from Prostrap Takeda Uk Limited (United Kingdom) on May 3, 2016. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 508 This firm has 1 other import refusal on record.
Refusal details
- Date
- May 3, 2016
- Country
- United Kingdom
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 508