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FDA Import Refusal DM9-6011123-3/1/1 — Metrax Gmbh

Metrax Gmbh — FEI 3001417379

The FDA refused shipment DM9-6011123-3/1/1 from Metrax Gmbh (Germany) on Sep 26, 2006. The refused product falls under Devices — AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE). Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Sep 26, 2006
Country
Germany
Product Category
Devices
Product Code
74MKJ AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE)
Charges
118,508

Other import refusals

FDA data resources

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