FDA Import Refusal 275-1435124-9/3/12 — Aesculap AG

Aesculap AG — FEI 3002806315

The FDA refused shipment 275-1435124-9/3/12 from Aesculap AG (Germany) on Mar 16, 2011. The refused product falls under Devices — PROSTHESIS, INTERVERTEBRAL DISC. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Mar 16, 2011
Country
Germany
Product Category
Devices
Product Code
87MJO PROSTHESIS, INTERVERTEBRAL DISC
Charges
341

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.