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ODM

⚠️ Moderate Risk

FEI: 3038507055 • Paris 2e Arrondissement, Paris • FRANCE

FEI

FEI Number

3038507055

📍

Location

Paris 2e Arrondissement, Paris

🇫🇷

Country

FRANCE
🏢

Address

5 Rue D'Alexandrie, , Paris 2e Arrondissement, Paris, France

Moderate Risk

FDA Import Risk Assessment

46.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/4/2025
Latest Refusal
8/4/2025
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
76.6×20%
Frequency
20.0×10%
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

4762×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
8/4/2025
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
476NO REGISTR
Division of Southeast Imports (DSEI)
8/4/2025
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ODM's FDA import refusal history?

ODM (FEI: 3038507055) has 2 FDA import refusal record(s) in our database, spanning from 8/4/2025 to 8/4/2025.

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. ODM's FEI number is 3038507055.

What types of violations has ODM received?

ODM 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 ODM come from?

All FDA import refusal data for ODM 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.