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PROVITA NUTRITION AND HEALTH INC

⚠️ High Risk

FEI: 3013890369 • Port Coquitlam, British Columbia • CANADA

FEI

FEI Number

3013890369

📍

Location

Port Coquitlam, British Columbia

🇨🇦

Country

CANADA
🏢

Address

1102-1225 Kingsway Ave, , Port Coquitlam, British Columbia, Canada

High Risk

FDA Import Risk Assessment

51.9
LowModerateHighCritical

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

Statistics

4
Total Refusals
8
Unique Violations
11/24/2025
Latest Refusal
7/17/2023
Earliest Refusal

Score Breakdown

Violation Severity
57.6×40%
Refusal Volume
25.9×30%
Recency
97.1×20%
Frequency
17.0×10%
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

754×

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).

2183×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2602×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3202×

LACKS FIRM

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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3242×

NO ENGLISH

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)).

33002×

ALLERGEN

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

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.

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

Refusal History

DateProductViolationsDivision
11/24/2025
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
260FALSE
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/24/2025
54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
260FALSE
320LACKS FIRM
324NO ENGLISH
3300ALLERGEN
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/10/2025
54FCF99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Division of West Coast Imports (DWCI)
7/17/2023
54FCE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
2280DIRSEXMPT
3864NCONTACT
75UNAPPROVED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is PROVITA NUTRITION AND HEALTH INC's FDA import refusal history?

PROVITA NUTRITION AND HEALTH INC (FEI: 3013890369) has 4 FDA import refusal record(s) in our database, spanning from 7/17/2023 to 11/24/2025.

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. PROVITA NUTRITION AND HEALTH INC's FEI number is 3013890369.

What types of violations has PROVITA NUTRITION AND HEALTH INC received?

PROVITA NUTRITION AND HEALTH INC has been cited for 8 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 PROVITA NUTRITION AND HEALTH INC come from?

All FDA import refusal data for PROVITA NUTRITION AND HEALTH 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.