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FDA Import Refusal 799-2229635-6/11/1 — QUINTENZ HYBRIDTECHNIK GMBH

QUINTENZ HYBRIDTECHNIK GMBH — FEI 3010232390

The FDA refused shipment 799-2229635-6/11/1 from QUINTENZ HYBRIDTECHNIK GMBH (Germany) on Jul 30, 2024. The refused product falls under Devices — ORTHOPEDIC STEREOTAXIC INSTRUMENT. Cited charge: 3904

Refusal Details

Date
Jul 30, 2024
Country
Germany
Product Category
Devices
Product Code
87OLO ORTHOPEDIC STEREOTAXIC INSTRUMENT
Charges
3904

FDA data resources

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