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Mcintosh Pro Line

⚠️ Moderate Risk

FEI: 3003884698 • Wheatley, ON • CANADA

FEI

FEI Number

3003884698

📍

Location

Wheatley, ON

🇨🇦

Country

CANADA
🏢

Address

779 Kent Rd /#1 On, , Wheatley, ON, Canada

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
1/13/2012
Latest Refusal
5/3/2011
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

722×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
1/13/2012
68GYR02HORSES NUTRIENT
72NEW VET DR
Cincinnati District Office (CIN-DO)
5/3/2011
62GPR99ANTI-INFLAMMATORY N.E.C.
72NEW VET DR
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Mcintosh Pro Line's FDA import refusal history?

Mcintosh Pro Line (FEI: 3003884698) has 2 FDA import refusal record(s) in our database, spanning from 5/3/2011 to 1/13/2012.

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. Mcintosh Pro Line's FEI number is 3003884698.

What types of violations has Mcintosh Pro Line received?

Mcintosh Pro Line 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 Mcintosh Pro Line come from?

All FDA import refusal data for Mcintosh Pro Line 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.