ImportRefusal LogoImportRefusal

Phoenix Bio-Tech Corporation

⚠️ Moderate Risk

FEI: 3000178022 • Mississauga, Ontario • CANADA

FEI

FEI Number

3000178022

📍

Location

Mississauga, Ontario

🇨🇦

Country

CANADA
🏢

Address

6810 Kitimat Rd Unit 4, , Mississauga, Ontario, Canada

Moderate Risk

FDA Import Risk Assessment

32.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
12/11/2003
Latest Refusal
6/12/2002
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
13.3×10%
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

1181×

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).

27801×

DEVICEGMPS

The article is subject to refusal of admission pursuant to Section 801(a)(1) in that the methods used in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the device do not conform to the requirements of Section 520(f)(1) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) or a condition prescribed by an order under section 520(f)(2) of the FD&C Act.

5081×

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.

Refusal History

DateProductViolationsDivision
12/11/2003
81MTNTEST, SYPHILIS, TREPONEMAL
118NOT LISTED
508NO 510(K)
New York District Office (NYK-DO)
6/12/2002
57YY99BIOLOGICAL IN-VIVO AND IN-VITRO DIAGNOSTICS, N.E.C.
2780DEVICEGMPS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Phoenix Bio-Tech Corporation's FDA import refusal history?

Phoenix Bio-Tech Corporation (FEI: 3000178022) has 2 FDA import refusal record(s) in our database, spanning from 6/12/2002 to 12/11/2003.

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. Phoenix Bio-Tech Corporation's FEI number is 3000178022.

What types of violations has Phoenix Bio-Tech Corporation received?

Phoenix Bio-Tech Corporation 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 Phoenix Bio-Tech Corporation come from?

All FDA import refusal data for Phoenix Bio-Tech Corporation 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.