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2187954 ALBERTA INC.

⚠️ High Risk

FEI: 3027888319 • Lethbridge, Alberta • CANADA

FEI

FEI Number

3027888319

📍

Location

Lethbridge, Alberta

🇨🇦

Country

CANADA
🏢

Address

Suite 162-210A 12A St N, , Lethbridge, Alberta, Canada

High Risk

FDA Import Risk Assessment

61.5
LowModerateHighCritical

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

Statistics

7
Total Refusals
1
Unique Violations
11/7/2023
Latest Refusal
10/31/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
33.5×30%
Recency
42.1×20%
Frequency
70.0×10%
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

757×

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
11/7/2023
60BDR01AMMONIUM CHLORIDE (ACIDIFIER)
75UNAPPROVED
Division of West Coast Imports (DWCI)
11/7/2023
60BDR01AMMONIUM CHLORIDE (ACIDIFIER)
75UNAPPROVED
Division of West Coast Imports (DWCI)
11/7/2023
60BDR01AMMONIUM CHLORIDE (ACIDIFIER)
75UNAPPROVED
Division of West Coast Imports (DWCI)
11/7/2023
60BDR01AMMONIUM CHLORIDE (ACIDIFIER)
75UNAPPROVED
Division of West Coast Imports (DWCI)
10/31/2023
66BAY30AMMONIA SPIRIT, AROMMATIC (STIMULANT)
75UNAPPROVED
Division of West Coast Imports (DWCI)
10/31/2023
66BAY30AMMONIA SPIRIT, AROMMATIC (STIMULANT)
75UNAPPROVED
Division of West Coast Imports (DWCI)
10/31/2023
60BDR01AMMONIUM CHLORIDE (ACIDIFIER)
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is 2187954 ALBERTA INC.'s FDA import refusal history?

2187954 ALBERTA INC. (FEI: 3027888319) has 7 FDA import refusal record(s) in our database, spanning from 10/31/2023 to 11/7/2023.

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. 2187954 ALBERTA INC.'s FEI number is 3027888319.

What types of violations has 2187954 ALBERTA INC. received?

2187954 ALBERTA 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 2187954 ALBERTA INC. come from?

All FDA import refusal data for 2187954 ALBERTA 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.