ImportRefusal LogoImportRefusal

Dextran Products Ltd

⚠️ High Risk

FEI: 3001860609 • Scarborough, Ontario • CANADA

FEI

FEI Number

3001860609

📍

Location

Scarborough, Ontario

🇨🇦

Country

CANADA
🏢

Address

421-423 Comstock Rd, , Scarborough, Ontario, Canada

High Risk

FDA Import Risk Assessment

54.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
6/5/2025
Latest Refusal
6/5/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
88.0×20%
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

721×

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
6/5/2025
64NDK07IRON DEXTRAN (INJ) (HEMATINIC)
72NEW VET DR
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Dextran Products Ltd's FDA import refusal history?

Dextran Products Ltd (FEI: 3001860609) has 1 FDA import refusal record(s) in our database, spanning from 6/5/2025 to 6/5/2025.

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. Dextran Products Ltd's FEI number is 3001860609.

What types of violations has Dextran Products Ltd received?

Dextran Products Ltd 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 Dextran Products Ltd come from?

All FDA import refusal data for Dextran Products Ltd 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.