Luxottica Group S.P.A.
⚠️ Moderate Risk
FEI: 3009586234 • Sedico, Belluno • ITALY
FEI Number
3009586234
Location
Sedico, Belluno
Country
ITALYAddress
Via Villa 2/A, , Sedico, Belluno, Italy
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/26/2023 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | 3280FRNMFGREG | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Luxottica Group S.P.A.'s FDA import refusal history?
Luxottica Group S.P.A. (FEI: 3009586234) has 1 FDA import refusal record(s) in our database, spanning from 5/26/2023 to 5/26/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Luxottica Group S.P.A.'s FEI number is 3009586234.
What types of violations has Luxottica Group S.P.A. received?
Luxottica Group S.P.A. has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Luxottica Group S.P.A. come from?
All FDA import refusal data for Luxottica Group S.P.A. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.