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Idbio

⚠️ Moderate Risk

FEI: 3003872925 • Saint-Hyacinthe, QC • CANADA

FEI

FEI Number

3003872925

📍

Location

Saint-Hyacinthe, QC

🇨🇦

Country

CANADA
🏢

Address

4395 Ave Beaudry, , Saint-Hyacinthe, QC, Canada

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
3/14/2003
Latest Refusal
3/14/2003
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

22021×

INSAN BSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
3/14/2003
54G01BOVINE (COW, ETC.) (ANIMAL BY-PRODUCTS AND EXTRACTS)
2202INSAN BSE
249FILTHY
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Idbio's FDA import refusal history?

Idbio (FEI: 3003872925) has 1 FDA import refusal record(s) in our database, spanning from 3/14/2003 to 3/14/2003.

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. Idbio's FEI number is 3003872925.

What types of violations has Idbio received?

Idbio 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 Idbio come from?

All FDA import refusal data for Idbio 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.