LES FROMAGERS DE TRADITION
⚠️ Moderate Risk
FEI: 3005053910 • Noyal Sur Vilaine, Ille-et-Vilaine • FRANCE
FEI Number
3005053910
Location
Noyal Sur Vilaine, Ille-et-Vilaine
Country
FRANCEAddress
La Riviere, , Noyal Sur Vilaine, Ille-et-Vilaine, France
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
LISTERIA
The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.
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)).
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.
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.
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/31/2012 | 12CGP12SOFT RIPENED CHEESE MADE FROM GOAT'S MILK (E.G., CHEVRE, FETA, GOAT) | San Francisco District Office (SAN-DO) | |
| 10/2/2012 | 12CGP12SOFT RIPENED CHEESE MADE FROM GOAT'S MILK (E.G., CHEVRE, FETA, GOAT) | 324NO ENGLISH | San Francisco District Office (SAN-DO) |
| 9/27/2012 | 12CGO12SOFT RIPENED CHEESE MADE FROM GOAT'S MILK (E.G., CHEVRE, FETA, GOAT) | Division of Northeast Imports (DNEI) | |
| 8/26/2010 | 12CGP15CHEESE, GOAT, N.E.C. | New England District Office (NWE-DO) | |
| 12/6/2006 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 308MFR INSAN | New York District Office (NYK-DO) |
| 1/14/2004 | 12CGP15CHEESE, GOAT, N.E.C. | 295LISTERIA | New York District Office (NYK-DO) |
| 1/14/2004 | 12CGP15CHEESE, GOAT, N.E.C. | 295LISTERIA | New York District Office (NYK-DO) |
| 6/26/2003 | 12AFP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New York District Office (NYK-DO) |
| 12/19/2002 | 12CGP15CHEESE, GOAT, N.E.C. | 295LISTERIA | New York District Office (NYK-DO) |
Frequently Asked Questions
What is LES FROMAGERS DE TRADITION's FDA import refusal history?
LES FROMAGERS DE TRADITION (FEI: 3005053910) has 9 FDA import refusal record(s) in our database, spanning from 12/19/2002 to 12/31/2012.
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. LES FROMAGERS DE TRADITION's FEI number is 3005053910.
What types of violations has LES FROMAGERS DE TRADITION received?
LES FROMAGERS DE TRADITION 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 LES FROMAGERS DE TRADITION come from?
All FDA import refusal data for LES FROMAGERS DE TRADITION 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.