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FDA Import Refusal AEK-0700754-4/10002/1 — Citieffe Srl

Citieffe Srl — FEI 3003249380

The FDA refused shipment AEK-0700754-4/10002/1 from Citieffe Srl (Italy) on Jul 7, 2026. The refused product falls under Devices — ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES. Cited charges: 118,476

Refusal details

Date
Jul 7, 2026
Country
Italy
Product Category
Devices
Product Code
87HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
Charges
118,476

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FDA data resources

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