ImportRefusal LogoImportRefusal

Jamieson Laboratories

⚠️ High Risk

FEI: 3004296668 • Toronto, Ontario • CANADA

FEI

FEI Number

3004296668

📍

Location

Toronto, Ontario

🇨🇦

Country

CANADA
🏢

Address

2 St Clair Ave W 16 Th Floor, , Toronto, Ontario, Canada

High Risk

FDA Import Risk Assessment

52.9
LowModerateHighCritical

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

Statistics

12
Total Refusals
9
Unique Violations
9/19/2025
Latest Refusal
1/27/2006
Earliest Refusal

Score Breakdown

Violation Severity
52.8×40%
Refusal Volume
41.3×30%
Recency
93.8×20%
Frequency
6.1×10%
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

4828×

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.

755×

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).

38645×

NCONTACT

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(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

23004×

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.

38623×

DIETARYING

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)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2561×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

Refusal History

DateProductViolationsDivision
9/19/2025
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
3862DIETARYING
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Northern Border Imports (DNBI)
9/19/2025
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
3862DIETARYING
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Northern Border Imports (DNBI)
9/19/2025
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
3862DIETARYING
3864NCONTACT
482NUTRIT LBL
75UNAPPROVED
Division of Northern Border Imports (DNBI)
3/2/2023
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3300ALLERGEN
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
1/23/2017
54ABC99VITAMIN, N.E.C.
3864NCONTACT
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/7/2016
54HYY05OMEGA-3 (FATS AND LIPID SUBSTANCES)
482NUTRIT LBL
New Orleans District Office (NOL-DO)
5/27/2016
54AEE99VITAMIN, N.E.C.
2300DIETARYLBL
3864NCONTACT
482NUTRIT LBL
488HEALTH C
Division of Southeast Imports (DSEI)
1/7/2015
54FYF99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Minneapolis District Office (MIN-DO)
1/27/2006
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
New Orleans District Office (NOL-DO)
1/27/2006
03MFT02CHOCOLATE COOKIE, BISCUIT, WAFER DOUGH
473LABELING
New Orleans District Office (NOL-DO)
1/27/2006
54YYY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
256INCONSPICU
New Orleans District Office (NOL-DO)
1/27/2006
66JCY01LEVOTHYROXINE SODIUM (THYROID HORMONE)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Jamieson Laboratories's FDA import refusal history?

Jamieson Laboratories (FEI: 3004296668) has 12 FDA import refusal record(s) in our database, spanning from 1/27/2006 to 9/19/2025.

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. Jamieson Laboratories's FEI number is 3004296668.

What types of violations has Jamieson Laboratories received?

Jamieson Laboratories has been cited for 9 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 Jamieson Laboratories come from?

All FDA import refusal data for Jamieson Laboratories 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.