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Nigerian Breweries Plc

⚠️ Moderate Risk

FEI: 3000136162 • Lagos, Lagos State • NIGERIA

FEI

FEI Number

3000136162

📍

Location

Lagos, Lagos State

🇳🇬

Country

NIGERIA
🏢

Address

1 Abebe Village Rd., , Lagos, Lagos State, Nigeria

Moderate Risk

FDA Import Risk Assessment

28.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
2/12/2003
Latest Refusal
2/12/2003
Earliest Refusal

Score Breakdown

Violation Severity
40.6×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2184×

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.

4734×

LABELING

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

4824×

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.

3283×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
2/12/2003
29CCT99NONALCOHOLIC BEVERAGES, N.E.C.
218LIST INGRE
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
2/12/2003
29CYY99NONALCOHOLIC BEVERAGES, N.E.C.
218LIST INGRE
328USUAL NAME
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
2/12/2003
29CYY99NONALCOHOLIC BEVERAGES, N.E.C.
218LIST INGRE
328USUAL NAME
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)
2/12/2003
29CYY99NONALCOHOLIC BEVERAGES, N.E.C.
218LIST INGRE
260FALSE
328USUAL NAME
473LABELING
482NUTRIT LBL
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Nigerian Breweries Plc's FDA import refusal history?

Nigerian Breweries Plc (FEI: 3000136162) has 4 FDA import refusal record(s) in our database, spanning from 2/12/2003 to 2/12/2003.

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. Nigerian Breweries Plc's FEI number is 3000136162.

What types of violations has Nigerian Breweries Plc received?

Nigerian Breweries Plc has been cited for 5 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 Nigerian Breweries Plc come from?

All FDA import refusal data for Nigerian Breweries Plc 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.