FDA Import Refusal AEK-3250749-1/41/1 — Luxottica Group S.P.A.
The FDA refused shipment AEK-3250749-1/41/1 from Luxottica Group S.P.A. (Italy) on May 26, 2023. The refused product falls under Devices — LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION). Cited charge: 3280 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- May 26, 2023
- Country
- Italy
- Product Category
- Devices
- Product Code
- 86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
- Charges
- 3280