FDA Import Refusal 799-0964781-4/16/1 — Dimeda Instrumente GmbH
The FDA refused shipment 799-0964781-4/16/1 from Dimeda Instrumente GmbH (Germany) on Nov 14, 2013. The refused product falls under Devices — STRIPPER, VEIN, REUSABLE. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Nov 14, 2013
- Country
- Germany
- Product Category
- Devices
- Product Code
- 79GAI STRIPPER, VEIN, REUSABLE
- Charges
- 118