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Amgen Canada Inc

⚠️ High Risk

FEI: 3006745676 • Mississauga, ON • CANADA

FEI

FEI Number

3006745676

📍

Location

Mississauga, ON

🇨🇦

Country

CANADA
🏢

Address

6775 Financial Drive Suite 100, , Mississauga, ON, Canada

High Risk

FDA Import Risk Assessment

72.7
LowModerateHighCritical

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

Statistics

16
Total Refusals
3
Unique Violations
12/10/2025
Latest Refusal
4/28/2023
Earliest Refusal

Score Breakdown

Violation Severity
83.3×40%
Refusal Volume
45.6×30%
Recency
98.1×20%
Frequency
61.0×10%
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

7515×

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).

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
12/10/2025
58SCK15ETANERCEPT
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/26/2025
62NCY99ANTI-PSORIATIC N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
11/14/2025
58SDP15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/23/2025
58SCY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2025
58SDY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/27/2025
62IDY31METHOTREXATE (ANTI-NEOPLASTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/21/2025
58SDY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/18/2025
58SDY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/13/2025
58SDY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/10/2024
58SCY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/9/2024
58SCK15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/9/2024
58SCK15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2024
58SCL15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/24/2024
58SCK15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/12/2024
58SCY15ETANERCEPT
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/28/2023
64ODK02DENOSUMAB, MONOCLONAL ANTIBODIES
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Amgen Canada Inc's FDA import refusal history?

Amgen Canada Inc (FEI: 3006745676) has 16 FDA import refusal record(s) in our database, spanning from 4/28/2023 to 12/10/2025.

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. Amgen Canada Inc's FEI number is 3006745676.

What types of violations has Amgen Canada Inc received?

Amgen Canada Inc has been cited for 3 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 Amgen Canada Inc come from?

All FDA import refusal data for Amgen Canada 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.