FDA Import Refusal 112-6162313-0/1/1 — Aesculap AG And Company KG
The FDA refused shipment 112-6162313-0/1/1 from Aesculap AG And Company KG (Germany) on Mar 29, 2017. The refused product falls under Devices — GRAFT, VASCULAR, BIOLOGICAL. Cited charge: 118
Refusal details
- Date
- Mar 29, 2017
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74MAK GRAFT, VASCULAR, BIOLOGICAL
- Charges
- 118