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Dr Ma's Laboratories, Inc.

⚠️ Moderate Risk

FEI: 3015391683 • Burnaby, British Columbia • CANADA

FEI

FEI Number

3015391683

📍

Location

Burnaby, British Columbia

🇨🇦

Country

CANADA
🏢

Address

4-8118 North Fraser Way, , Burnaby, British Columbia, Canada

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

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

Statistics

6
Total Refusals
5
Unique Violations
5/30/2025
Latest Refusal
7/20/2022
Earliest Refusal

Score Breakdown

Violation Severity
58.0×40%
Refusal Volume
31.3×30%
Recency
73.8×20%
Frequency
21.0×10%
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

35604×

SUPPL GMP

The article appears to be a dietary supplement and it has been prepared, packed, or held under conditions that do not meet current good manufacturing practice regulations.

4822×

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.

752×

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).

3251×

STD NAME

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(g)(2) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided under Section 401 of the FD&C Act and the article is not labeled with the name specified in the definition and standard, or the label does not bear the common names of optional ingredients (other than spices, flavoring and coloring) present in such food, insofar as may be required by such regulation.

38641×

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.

Refusal History

DateProductViolationsDivision
5/30/2025
54FCI33ASTRAGALUS (MILK VETCH ROOT), (HERBAL & BOTANICALS, NOT TEAS)
3560SUPPL GMP
75UNAPPROVED
Division of Northern Border Imports (DNBI)
5/30/2025
54KCI20MACA (HERBAL & BOTANICALS, NOT TEAS II)
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
5/30/2025
54FCI98BILBERRY (HERBAL & BOTANICALS, NOT TEAS)
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
5/14/2025
54FCY94ASHWAGANDHA (HERBAL & BOTANICALS, NOT TEAS)
3560SUPPL GMP
3864NCONTACT
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
1/30/2025
54FCF99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Division of West Coast Imports (DWCI)
7/20/2022
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
325STD NAME
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Dr Ma's Laboratories, Inc.'s FDA import refusal history?

Dr Ma's Laboratories, Inc. (FEI: 3015391683) has 6 FDA import refusal record(s) in our database, spanning from 7/20/2022 to 5/30/2025.

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. Dr Ma's Laboratories, Inc.'s FEI number is 3015391683.

What types of violations has Dr Ma's Laboratories, Inc. received?

Dr Ma's Laboratories, Inc. has been cited for 5 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 Dr Ma's Laboratories, Inc. come from?

All FDA import refusal data for Dr Ma's Laboratories, 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.