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FDA Import Refusal 112-0147402-6/1/1 — STERIS Deutschland GmbH

STERIS Deutschland GmbH — FEI 1000482681

The FDA refused shipment 112-0147402-6/1/1 from STERIS Deutschland GmbH (Germany) on Dec 21, 2012. The refused product falls under Devices — RONGEUR, MANUAL. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Dec 21, 2012
Country
Germany
Product Category
Devices
Product Code
84HAE RONGEUR, MANUAL
Charges
341

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FDA data resources

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