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Multi Laser

✅ Low Risk

FEI: 3003880704 • Drummondville, Quebec • CANADA

FEI

FEI Number

3003880704

📍

Location

Drummondville, Quebec

🇨🇦

Country

CANADA
🏢

Address

815 Saint-Joseph Blvd W, , Drummondville, Quebec, Canada

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
11/12/2004
Latest Refusal
11/12/2004
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4761×

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
11/12/2004
95L22LASER PRODUCT FOR NON-MEDICAL USE
336INCONSPICU
476NO REGISTR
New York District Office (NYK-DO)

Frequently Asked Questions

What is Multi Laser's FDA import refusal history?

Multi Laser (FEI: 3003880704) has 1 FDA import refusal record(s) in our database, spanning from 11/12/2004 to 11/12/2004.

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. Multi Laser's FEI number is 3003880704.

What types of violations has Multi Laser received?

Multi Laser 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 Multi Laser come from?

All FDA import refusal data for Multi Laser 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.