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UNILEVER MANUFACTURERA S DE RL D

⚠️ Moderate Risk

FEI: 3013088619 • TULTITLAN • MEXICO

FEI

FEI Number

3013088619

📍

Location

TULTITLAN

🇲🇽

Country

MEXICO
🏢

Address

TEPALCAPA NO 2 COL RANC, , TULTITLAN, , Mexico

Moderate Risk

FDA Import Risk Assessment

36.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
2/20/2025
Latest Refusal
2/20/2025
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
82.0×20%
Frequency
10.0×10%
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

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4731×

LABELING

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

Refusal History

DateProductViolationsDivision
2/20/2025
53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
473LABELING
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is UNILEVER MANUFACTURERA S DE RL D's FDA import refusal history?

UNILEVER MANUFACTURERA S DE RL D (FEI: 3013088619) has 1 FDA import refusal record(s) in our database, spanning from 2/20/2025 to 2/20/2025.

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. UNILEVER MANUFACTURERA S DE RL D's FEI number is 3013088619.

What types of violations has UNILEVER MANUFACTURERA S DE RL D received?

UNILEVER MANUFACTURERA S DE RL D has been cited for 2 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 MANUFACTURERA S DE RL D come from?

All FDA import refusal data for UNILEVER MANUFACTURERA S DE RL D 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.