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FDA Import Refusal 112-5874811-4/1/1 — Herman Medizintechnik

Herman Medizintechnik — FEI 3002452499

The FDA refused shipment 112-5874811-4/1/1 from Herman Medizintechnik (Germany) on Jan 7, 2012. The refused product falls under Devices — GUIDEWIRE, PERIPHERAL ABLATIVE. Cited charge: 118

Refusal details

Date
Jan 7, 2012
Country
Germany
Product Category
Devices
Product Code
74MKI GUIDEWIRE, PERIPHERAL ABLATIVE
Charges
118

FDA data resources

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