Elixir Global Manufacturing Food Limited
⚠️ High Risk
FEI: 3033056570 • Ibadan, Nigeria • NIGERIA
FEI Number
3033056570
Location
Ibadan, Nigeria
Country
NIGERIAAddress
First Commercial Road, Oluyole Industrial Estate, Ibadan, Nigeria, Nigeria
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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.
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
INCONSPICU
Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/13/2025 | 33YGT99CANDY WITHOUT CHOCOLATE N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/6/2025 | 34HET99CHOCOLATE AND COCOA BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/12/2025 | 34HHT99CHOCOLATE AND COCOA BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 6/12/2025 | 34HHT99CHOCOLATE AND COCOA BEVERAGE BASE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/11/2025 | 66YBT99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 3/11/2025 | 66YBT99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 12/31/2024 | 62MBY08MENTHOL (ANTI-PRURITIC) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Elixir Global Manufacturing Food Limited's FDA import refusal history?
Elixir Global Manufacturing Food Limited (FEI: 3033056570) has 7 FDA import refusal record(s) in our database, spanning from 12/31/2024 to 12/13/2025.
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 3033056570.
What types of violations has Elixir Global Manufacturing Food Limited received?
Elixir Global Manufacturing Food Limited has been cited for 9 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.