FDA Import Refusal K51-0072024-9/1/1 — Medtec
The FDA refused shipment K51-0072024-9/1/1 from Medtec (Germany) on Jul 19, 2011. The refused product falls under Devices — GENERATOR, HIGH-VOLTAGE, X-RAY, DIAGNOSTIC. Cited charge: 118 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jul 19, 2011
- Country
- Germany
- Product Category
- Devices
- Product Code
- 90IZO GENERATOR, HIGH-VOLTAGE, X-RAY, DIAGNOSTIC
- Charges
- 118