ImportRefusal LogoImportRefusal

UNILEVER ITALIA MANUFACTURING SRL LO

⚠️ Moderate Risk

FEI: 3024350317 • Casalpusterlengo, Lodi • ITALY

FEI

FEI Number

3024350317

📍

Location

Casalpusterlengo, Lodi

🇮🇹

Country

ITALY
🏢

Address

Via Lever Gibbs 4, , Casalpusterlengo, Lodi, Italy

Moderate Risk

FDA Import Risk Assessment

31.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/12/2023
Latest Refusal
12/12/2023
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
57.9×20%
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
12/12/2023
53JA02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is UNILEVER ITALIA MANUFACTURING SRL LO's FDA import refusal history?

UNILEVER ITALIA MANUFACTURING SRL LO (FEI: 3024350317) has 1 FDA import refusal record(s) in our database, spanning from 12/12/2023 to 12/12/2023.

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 ITALIA MANUFACTURING SRL LO's FEI number is 3024350317.

What types of violations has UNILEVER ITALIA MANUFACTURING SRL LO received?

UNILEVER ITALIA MANUFACTURING SRL LO 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 ITALIA MANUFACTURING SRL LO come from?

All FDA import refusal data for UNILEVER ITALIA MANUFACTURING SRL LO 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.