PRODUITS ANDALOS INC.
⚠️ Moderate Risk
FEI: 3004276899 • Saint-Laurent, Quebec • CANADA
FEI Number
3004276899
Location
Saint-Laurent, Quebec
Country
CANADAAddress
230 Lebeau Blvd, , Saint-Laurent, Quebec, Canada
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
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.
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.
USUAL 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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/5/2008 | 07AGT01BREAD STICKS (FLAVORED OR UNFLAVORED), BAKED | New England District Office (NWE-DO) | |
| 11/5/2008 | 03AGN14CROISSANT BREAD/ROLLS | New England District Office (NWE-DO) | |
| 11/5/2008 | 03RGT25PASTRY (OTHER THAN FRUIT OR JELLY FILLED) WITHOUT CUSTARD OR CREAM FILLING | New England District Office (NWE-DO) | |
| 11/5/2008 | 03RGT25PASTRY (OTHER THAN FRUIT OR JELLY FILLED) WITHOUT CUSTARD OR CREAM FILLING | New England District Office (NWE-DO) | |
| 11/5/2008 | 03AGT09NON-STANDARD BREAD/ROLLS/BUNS | New England District Office (NWE-DO) |
Frequently Asked Questions
What is PRODUITS ANDALOS INC.'s FDA import refusal history?
PRODUITS ANDALOS INC. (FEI: 3004276899) has 5 FDA import refusal record(s) in our database, spanning from 11/5/2008 to 11/5/2008.
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. PRODUITS ANDALOS INC.'s FEI number is 3004276899.
What types of violations has PRODUITS ANDALOS INC. received?
PRODUITS ANDALOS 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 PRODUITS ANDALOS INC. come from?
All FDA import refusal data for PRODUITS ANDALOS 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.