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Autolog Production Management Inc

⚠️ Moderate Risk

FEI: 3003199267 • Blainville, Quebec • CANADA

FEI

FEI Number

3003199267

📍

Location

Blainville, Quebec

🇨🇦

Country

CANADA
🏢

Address

1240 Boul Michele Bohec, , Blainville, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/28/2006
Latest Refusal
9/28/2006
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
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
9/28/2006
95L22LASER PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
Detroit District Office (DET-DO)
9/28/2006
95L22LASER PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Autolog Production Management Inc's FDA import refusal history?

Autolog Production Management Inc (FEI: 3003199267) has 2 FDA import refusal record(s) in our database, spanning from 9/28/2006 to 9/28/2006.

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. Autolog Production Management Inc's FEI number is 3003199267.

What types of violations has Autolog Production Management Inc received?

Autolog Production Management Inc 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 Autolog Production Management Inc come from?

All FDA import refusal data for Autolog Production Management Inc 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.