Orlux
⚠️ Moderate Risk
FEI: 3009328803 • Astene, Oost-Vlaanderen • BELGIUM
FEI Number
3009328803
Location
Astene, Oost-Vlaanderen
Country
BELGIUMAddress
Kapellestraat 70, , Astene, Oost-Vlaanderen, Belgium
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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/6/2012 | 72CGT99PET BIRD FOOD N.E.C. | New York District Office (NYK-DO) | |
| 3/6/2012 | 72CHT99PET BIRD FOOD N.E.C. | New York District Office (NYK-DO) | |
| 3/6/2012 | 72CGB99PET BIRD FOOD N.E.C. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Orlux's FDA import refusal history?
Orlux (FEI: 3009328803) has 3 FDA import refusal record(s) in our database, spanning from 3/6/2012 to 3/6/2012.
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. Orlux's FEI number is 3009328803.
What types of violations has Orlux received?
Orlux has been cited for 2 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 Orlux come from?
All FDA import refusal data for Orlux 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.