Elixir Global Manufacturing Food Limited
⚠️ Moderate Risk
FEI: 3040979298 • Lagos, Lagos • NIGERIA
FEI Number
3040979298
Location
Lagos, Lagos
Country
NIGERIAAddress
5/6 Kopek Street, Fatai Atere Way St., Lagos, Lagos, Nigeria
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
Frequently Asked Questions
What is Elixir Global Manufacturing Food Limited's FDA import refusal history?
Elixir Global Manufacturing Food Limited (FEI: 3040979298) has 3 FDA import refusal record(s) in our database, spanning from 12/5/2025 to 12/5/2025.
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. Elixir Global Manufacturing Food Limited's FEI number is 3040979298.
What types of violations has Elixir Global Manufacturing Food Limited received?
Elixir Global Manufacturing Food Limited 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 Elixir Global Manufacturing Food Limited come from?
All FDA import refusal data for Elixir Global Manufacturing Food Limited 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.