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Odu Chig Investment Limited

⚠️ Moderate Risk

FEI: 3005140747 • Ikeja • NIGERIA

FEI

FEI Number

3005140747

📍

Location

Ikeja

🇳🇬

Country

NIGERIA
🏢

Address

Plot 70 New Isheri Road Ojodu, , Ikeja, , Nigeria

Moderate Risk

FDA Import Risk Assessment

37.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

6
Total Refusals
8
Unique Violations
12/8/2006
Latest Refusal
2/21/2006
Earliest Refusal

Score Breakdown

Violation Severity
56.1×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
60.0×10%
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

3213×

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.

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

2182×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

3201×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
12/8/2006
24BFT99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE)
249FILTHY
Los Angeles District Office (LOS-DO)
12/8/2006
24BFT99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE)
249FILTHY
Los Angeles District Office (LOS-DO)
12/8/2006
38PFH28MIXED VEGETABLE BROTH, DRIED
218LIST INGRE
Los Angeles District Office (LOS-DO)
2/21/2006
24HEH50TOMATO, DRIED
321LACKS N/C
324NO ENGLISH
Los Angeles District Office (LOS-DO)
2/21/2006
23BCH07PEANUT, SHELLED
249FILTHY
320LACKS FIRM
321LACKS N/C
473LABELING
Los Angeles District Office (LOS-DO)
2/21/2006
21VHY24PALM NUT (PALM FRUIT, SUGAR PALM), JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
218LIST INGRE
321LACKS N/C
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Odu Chig Investment Limited's FDA import refusal history?

Odu Chig Investment Limited (FEI: 3005140747) has 6 FDA import refusal record(s) in our database, spanning from 2/21/2006 to 12/8/2006.

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. Odu Chig Investment Limited's FEI number is 3005140747.

What types of violations has Odu Chig Investment Limited received?

Odu Chig Investment Limited has been cited for 8 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 Odu Chig Investment Limited come from?

All FDA import refusal data for Odu Chig Investment 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.