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Pharmalab 1982 Inc. Dba. Ideal Protein

⚠️ High Risk

FEI: 3007972013 • Levis, Quebec • CANADA

FEI

FEI Number

3007972013

📍

Location

Levis, Quebec

🇨🇦

Country

CANADA
🏢

Address

8750 Guillaume-Couture Blvd, , Levis, Quebec, Canada

High Risk

FDA Import Risk Assessment

52.7
LowModerateHighCritical

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

Statistics

23
Total Refusals
11
Unique Violations
9/20/2023
Latest Refusal
12/19/2006
Earliest Refusal

Score Breakdown

Violation Severity
63.1×40%
Refusal Volume
51.1×30%
Recency
53.8×20%
Frequency
13.7×10%
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

2385×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

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.

2184×

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.

2603×

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.

26403×

CYCLAMATE

The article appears to bear or contain cyclamate, an unsafe food additive within the meaning of Section 409

23002×

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.

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

3201×

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.

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.

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.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

Refusal History

DateProductViolationsDivision
9/20/2023
54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
9/20/2023
54ACY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
9/20/2023
54YBL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
9/20/2023
54YBL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
3560SUPPL GMP
Division of Northern Border Imports (DNBI)
1/8/2018
12AVT05CHEESE, CHEDDAR
218LIST INGRE
320LACKS FIRM
Division of Northern Border Imports (DNBI)
5/20/2017
36DGT01IMITATION MAPLE SYRUP
62NEEDS FCE
83NO PROCESS
Division of Northern Border Imports (DNBI)
6/27/2011
03SFT23PANCAKE PREPARED DRY MIX WITHOUT CUSTARD OR CREAM FILLING
2640CYCLAMATE
New England District Office (NWE-DO)
11/9/2009
54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
New England District Office (NWE-DO)
7/27/2009
35DFT04CHOCOLATE PUDDING (PIE FILLING) MIX (NOT CUSTARD)
260FALSE
New York District Office (NYK-DO)
7/27/2009
41BGT99FOODS WITH SUPPLEMENTAL NUTRIENTS ADDED, WITH OR WITHOUT ARTIFICAL SWEETNERS
260FALSE
New York District Office (NYK-DO)
7/27/2009
35DGT02BUTTERSCOTCH PUDDING (PIE FILLING) MIX (NOT CUSTARD)
260FALSE
New York District Office (NYK-DO)
6/10/2009
35AFT01GELATIN, FLAVORED
218LIST INGRE
New York District Office (NYK-DO)
6/10/2009
35DFT02BUTTERSCOTCH PUDDING (PIE FILLING) MIX (NOT CUSTARD)
218LIST INGRE
New York District Office (NYK-DO)
10/14/2008
54BEA01CALCIUM (MINERAL)
218LIST INGRE
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
2300DIETARYLBL
488HEALTH C
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
238UNSAFE ADD
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
238UNSAFE ADD
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
238UNSAFE ADD
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
238UNSAFE ADD
New England District Office (NWE-DO)
2/7/2008
41GET02NUTRTIONALLY INCOMPLETE FORMULATIONS (PROTEIN, CARBOHYDRATE OR FAT MODULARS)
238UNSAFE ADD
New England District Office (NWE-DO)
1/17/2008
03SFB23PANCAKE PREPARED DRY MIX WITHOUT CUSTARD OR CREAM FILLING
2640CYCLAMATE
New York District Office (NYK-DO)
1/17/2008
03SAB01CAKE PREPARED DRY MIX WITHOUT CUSTARD OR CREAM FILLING
2640CYCLAMATE
New York District Office (NYK-DO)
12/19/2006
54CCR99PROTEIN N.E.C.
2300DIETARYLBL
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Pharmalab 1982 Inc. Dba. Ideal Protein's FDA import refusal history?

Pharmalab 1982 Inc. Dba. Ideal Protein (FEI: 3007972013) has 23 FDA import refusal record(s) in our database, spanning from 12/19/2006 to 9/20/2023.

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. Pharmalab 1982 Inc. Dba. Ideal Protein's FEI number is 3007972013.

What types of violations has Pharmalab 1982 Inc. Dba. Ideal Protein received?

Pharmalab 1982 Inc. Dba. Ideal Protein has been cited for 11 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 Pharmalab 1982 Inc. Dba. Ideal Protein come from?

All FDA import refusal data for Pharmalab 1982 Inc. Dba. Ideal Protein 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.