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FDA Import Refusal 799-7969616-8/11/1 — NUVASIVE NETHERLANDS

NUVASIVE NETHERLANDS — FEI 3012895001

The FDA refused shipment 799-7969616-8/11/1 from NUVASIVE NETHERLANDS (Netherlands) on Dec 4, 2023. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charges: 118,3280,508

Refusal details

Date
Dec 4, 2023
Country
Netherlands
Product Category
Devices
Product Code
80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
Charges
118,3280,508

FDA data resources

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