ImportRefusal LogoImportRefusal

Unilever Brasil Industrial

⚠️ Moderate Risk

FEI: 3015438668 • Pouso Alegre, Minas Gerais • BRAZIL

FEI

FEI Number

3015438668

📍

Location

Pouso Alegre, Minas Gerais

🇧🇷

Country

BRAZIL
🏢

Address

Avenida Prefeito Olavo Gomes Oliveira, 3701, , Pouso Alegre, Minas Gerais, Brazil

Moderate Risk

FDA Import Risk Assessment

40.4
LowModerateHighCritical

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

Statistics

10
Total Refusals
5
Unique Violations
6/7/2022
Latest Refusal
8/21/2019
Earliest Refusal

Score Breakdown

Violation Severity
56.1×40%
Refusal Volume
38.6×30%
Recency
13.9×20%
Frequency
35.8×10%
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

838×

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.

2565×

INCONSPICU

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)).

3242×

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)).

4822×

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.

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).

Refusal History

DateProductViolationsDivision
6/7/2022
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
62NEEDS FCE
83NO PROCESS
Division of Southeast Imports (DSEI)
9/7/2021
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
256INCONSPICU
83NO PROCESS
Division of Southeast Imports (DSEI)
9/7/2021
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
256INCONSPICU
83NO PROCESS
Division of Southeast Imports (DSEI)
9/7/2021
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
256INCONSPICU
83NO PROCESS
Division of Southeast Imports (DSEI)
9/7/2021
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
256INCONSPICU
83NO PROCESS
Division of Southeast Imports (DSEI)
9/7/2021
24DFF13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD'), JUICE OR DRINK
256INCONSPICU
83NO PROCESS
Division of Southeast Imports (DSEI)
3/9/2021
02HGT02CORN STARCH
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
3/9/2021
02HGT02CORN STARCH
324NO ENGLISH
482NUTRIT LBL
Division of Southeast Imports (DSEI)
8/21/2019
24JFF99FRUITS USED AS VEGETABLES, JUICE, N.E.C.
83NO PROCESS
Division of Southeast Imports (DSEI)
8/21/2019
21DFF99MIXED FRUIT, JUICES OR CONCENTRATES N.E.C.,
83NO PROCESS
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Unilever Brasil Industrial's FDA import refusal history?

Unilever Brasil Industrial (FEI: 3015438668) has 10 FDA import refusal record(s) in our database, spanning from 8/21/2019 to 6/7/2022.

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. Unilever Brasil Industrial's FEI number is 3015438668.

What types of violations has Unilever Brasil Industrial received?

Unilever Brasil Industrial 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 Unilever Brasil Industrial come from?

All FDA import refusal data for Unilever Brasil Industrial 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.