FDA Import Refusal AEK-3630448-0/11/1 — Karl Storz SE & Co. KG
The FDA refused shipment AEK-3630448-0/11/1 from Karl Storz SE & Co. KG (Germany) on Aug 29, 2017. The refused product falls under Devices — DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES. Cited charge: 341 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 29, 2017
- Country
- Germany
- Product Category
- Devices
- Product Code
- 79GEI DEVICE, ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
- Charges
- 341