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FDA Import Refusal AEK-7971559-2/11/1 — Stryker Trauma GmbH

Stryker Trauma GmbH — FEI 3002807231

The FDA refused shipment AEK-7971559-2/11/1 from Stryker Trauma GmbH (Germany) on Dec 9, 2020. The refused product falls under Devices — ORTHOPEDIC MANUAL SURGICAL INSTRUMENT. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 9, 2020
Country
Germany
Product Category
Devices
Product Code
87LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Charges
118

Other import refusals

FDA data resources

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