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Response Biomedical Corp.

⚠️ Moderate Risk

FEI: 3004205692 • Vancouver, British Columbia • CANADA

FEI

FEI Number

3004205692

📍

Location

Vancouver, British Columbia

🇨🇦

Country

CANADA
🏢

Address

1781 75th Ave W, , Vancouver, British Columbia, Canada

Moderate Risk

FDA Import Risk Assessment

45.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
11/28/2025
Latest Refusal
9/22/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
17.7×30%
Recency
97.6×20%
Frequency
3.9×10%
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

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).

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

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.

39051×

3905

Refusal History

DateProductViolationsDivision
11/28/2025
88PPMGENERAL PURPOSE REAGENT
118NOT LISTED
3280FRNMFGREG
39053905
508NO 510(K)
Division of Southeast Imports (DSEI)
9/22/2020
83PBKNON-VARIOLA ORTHOPOXVIRUS REAL-TIME PCR PRIMER AND PROBE SET
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Response Biomedical Corp.'s FDA import refusal history?

Response Biomedical Corp. (FEI: 3004205692) has 2 FDA import refusal record(s) in our database, spanning from 9/22/2020 to 11/28/2025.

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. Response Biomedical Corp.'s FEI number is 3004205692.

What types of violations has Response Biomedical Corp. received?

Response Biomedical Corp. has been cited for 4 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 Response Biomedical Corp. come from?

All FDA import refusal data for Response Biomedical Corp. 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.