FDA Import Refusal AEK-9637397-8/1/1 — Merz North America, Inc.
The FDA refused shipment AEK-9637397-8/1/1 from Merz North America, Inc. (United States) on Mar 17, 2010. The refused product falls under Devices — TRANSDUCER, ULTRASONIC, DIAGNOSTIC. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Mar 17, 2010
- Country
- United States
- Product Category
- Devices
- Product Code
- 90ITX TRANSDUCER, ULTRASONIC, DIAGNOSTIC
- Charges
- 341