FDA Import Refusal DM9-8011123-9/1/1 — Metrax Gmbh

Metrax Gmbh — FEI 3001417379

The FDA refused shipment DM9-8011123-9/1/1 from Metrax Gmbh (Germany) on Oct 20, 2008. The refused product falls under Devices — AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE). Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 20, 2008
Country
Germany
Product Category
Devices
Product Code
74MKJ AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE)
Charges
118

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