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MENELA GROUP LTDA

⚠️ Moderate Risk

FEI: 3032723970 • Limeira, Sao Paulo • BRAZIL

FEI

FEI Number

3032723970

📍

Location

Limeira, Sao Paulo

🇧🇷

Country

BRAZIL
🏢

Address

Rua Capitao Camargo, 250, , Limeira, Sao Paulo, Brazil

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/5/2024
Latest Refusal
12/5/2024
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
62.9×20%
Frequency
30.0×10%
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

4713×

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.

Refusal History

DateProductViolationsDivision
12/5/2024
53CD07EYELASH AND EYEBROW DYE (EYE MAKEUP PREPARATIONS)
471CSTIC LBLG
Division of Southeast Imports (DSEI)
12/5/2024
53CD07EYELASH AND EYEBROW DYE (EYE MAKEUP PREPARATIONS)
471CSTIC LBLG
Division of Southeast Imports (DSEI)
12/5/2024
53CD07EYELASH AND EYEBROW DYE (EYE MAKEUP PREPARATIONS)
471CSTIC LBLG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MENELA GROUP LTDA's FDA import refusal history?

MENELA GROUP LTDA (FEI: 3032723970) has 3 FDA import refusal record(s) in our database, spanning from 12/5/2024 to 12/5/2024.

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. MENELA GROUP LTDA's FEI number is 3032723970.

What types of violations has MENELA GROUP LTDA received?

MENELA GROUP LTDA has been cited for 1 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 MENELA GROUP LTDA come from?

All FDA import refusal data for MENELA GROUP LTDA 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.