FDA Import Refusal AEK-1267121-7/1/1 — Zimmer Medizinsysteme Gmbh
The FDA refused shipment AEK-1267121-7/1/1 from Zimmer Medizinsysteme Gmbh (Germany) on Jun 2, 2015. The refused product falls under Devices — GENERATOR, SHOCK-WAVE, (FOR PAIN RELIEF). Cited charges: 118,16,237,3280,341 This firm has 2 other import refusals on record.
Refusal Details
- Date
- Jun 2, 2015
- Country
- Germany
- Product Category
- Devices
- Product Code
- 87NBN GENERATOR, SHOCK-WAVE, (FOR PAIN RELIEF)
- Charges
- 118,16,237,3280,341