Les Maitres Laitiers du Cotentin
⚠️ Moderate Risk
FEI: 3004312903 • Sottevast, Manche • FRANCE
FEI Number
3004312903
Location
Sottevast, Manche
Country
FRANCEAddress
BP 102, , Sottevast, Manche, 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
NO PERMIT
The article of milk or cream is not accompanied by a valid import milk permit, as required by the Federal Import Milk Act (21 U.S.C. 141-149).
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
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.
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.
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.
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/11/2014 | 12AGP52CHEESE, SEMISOFT | 238UNSAFE ADD | New York District Office (NYK-DO) |
| 4/10/2014 | 12AGP52CHEESE, SEMISOFT | 11UNSAFE COL | New York District Office (NYK-DO) |
| 3/24/2014 | 12AGO52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 11/22/2011 | 12DHO95SKYR | New York District Office (NYK-DO) | |
| 4/1/2010 | 12AFO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | Seattle District Office (SEA-DO) |
| 5/8/2009 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 2/19/2004 | 09CYO95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
| 2/19/2004 | 09CYO95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
| 2/19/2004 | 09CYO95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
| 2/19/2004 | 09CYO95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
| 8/20/2003 | 12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 308MFR INSAN | Baltimore District Office (BLT-DO) |
| 5/19/2003 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 3/6/2002 | 09CEE95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
| 3/6/2002 | 09CYO95IMPORT MILK ACT | 156NO PERMIT | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Les Maitres Laitiers du Cotentin's FDA import refusal history?
Les Maitres Laitiers du Cotentin (FEI: 3004312903) has 14 FDA import refusal record(s) in our database, spanning from 3/6/2002 to 4/11/2014.
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 Maitres Laitiers du Cotentin's FEI number is 3004312903.
What types of violations has Les Maitres Laitiers du Cotentin received?
Les Maitres Laitiers du Cotentin 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 Les Maitres Laitiers du Cotentin come from?
All FDA import refusal data for Les Maitres Laitiers du Cotentin 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.