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Orion Group

⚠️ Moderate Risk

FEI: 3007841136 • Wolfville, Nova Scotia • CANADA

FEI

FEI Number

3007841136

📍

Location

Wolfville, Nova Scotia

🇨🇦

Country

CANADA
🏢

Address

53 King St, , Wolfville, Nova Scotia, Canada

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/11/2009
Latest Refusal
12/11/2009
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
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

33801×

EXPIRED

the product strength differs from, or its purity or quality falls below, that which it purports or is represented to possess in that it is past its labeled expiration date.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/11/2009
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
3380EXPIRED
75UNAPPROVED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Orion Group's FDA import refusal history?

Orion Group (FEI: 3007841136) has 1 FDA import refusal record(s) in our database, spanning from 12/11/2009 to 12/11/2009.

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. Orion Group's FEI number is 3007841136.

What types of violations has Orion Group received?

Orion Group 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 Orion Group come from?

All FDA import refusal data for Orion Group 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.