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Acenzia Inc.

⚠️ High Risk

FEI: 3008764049 • Oldcastle, Ontario • CANADA

FEI

FEI Number

3008764049

📍

Location

Oldcastle, Ontario

🇨🇦

Country

CANADA
🏢

Address

1580 Rossi Dr, , Oldcastle, Ontario, Canada

High Risk

FDA Import Risk Assessment

55.2
LowModerateHighCritical

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

Statistics

9
Total Refusals
6
Unique Violations
10/18/2024
Latest Refusal
12/18/2019
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
37.0×30%
Recency
61.2×20%
Frequency
18.6×10%
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).

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).

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

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.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
10/18/2024
54YCT99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
482NUTRIT LBL
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/3/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/3/2023
54CYC99PROTEIN N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/3/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/3/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/3/2023
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)
8/3/2022
54BYL06IODINE (MINERAL)
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
4/12/2022
54FCE50HAWTHORN (HERBAL & BOTANICALS, NOT TEAS)
308MFR INSAN
Division of Northern Border Imports (DNBI)
12/18/2019
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Acenzia Inc.'s FDA import refusal history?

Acenzia Inc. (FEI: 3008764049) has 9 FDA import refusal record(s) in our database, spanning from 12/18/2019 to 10/18/2024.

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. Acenzia Inc.'s FEI number is 3008764049.

What types of violations has Acenzia Inc. received?

Acenzia Inc. has been cited for 6 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 Acenzia Inc. come from?

All FDA import refusal data for Acenzia 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.