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FDA Import Refusal AEK-5974816-8/11/1 — Centervue Spa

Centervue Spa — FEI 3008422902

The FDA refused shipment AEK-5974816-8/11/1 from Centervue Spa (Italy) on Dec 6, 2024. The refused product falls under Devices — OPHTHALMOSCOPE, LASER, SCANNING. Cited charges: 341,476 This firm has 1 other import refusal on record.

Refusal Details

Date
Dec 6, 2024
Country
Italy
Product Category
Devices
Product Code
86MYC OPHTHALMOSCOPE, LASER, SCANNING
Charges
341,476

Other import refusals

FDA data resources

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