Dexpa
⚠️ High Risk
FEI: 1000603982 • Thiais, Val de Marne • FRANCE
FEI Number
1000603982
Location
Thiais, Val de Marne
Country
FRANCEAddress
5 Rue Des Hauts Flouviers, , Thiais, Val de Marne, France
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
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.
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.
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/19/2004 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | New England District Office (NWE-DO) | |
| 11/19/2004 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | New England District Office (NWE-DO) | |
| 11/19/2004 | 12AHP99CHEESE (STANDARDIZED),N.E.C. | New England District Office (NWE-DO) | |
| 11/19/2004 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | New England District Office (NWE-DO) | |
| 4/6/2004 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | Division of Northeast Imports (DNEI) |
| 4/6/2004 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | Division of Northeast Imports (DNEI) |
| 4/1/2004 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | New England District Office (NWE-DO) | |
| 4/1/2004 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | New England District Office (NWE-DO) | |
| 12/16/2003 | 12AGP16CHEESE, GOUDA | 324NO ENGLISH | New England District Office (NWE-DO) |
| 12/16/2003 | 12AGP52CHEESE, SEMISOFT | New England District Office (NWE-DO) | |
| 6/9/2003 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 6/9/2003 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 6/9/2003 | 12AGP52CHEESE, SEMISOFT | New York District Office (NYK-DO) | |
| 2/26/2003 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 2/26/2003 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 2/26/2003 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 7/11/2002 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New York District Office (NYK-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 12/10/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 11/20/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 11/20/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 11/20/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 11/20/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 11/20/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 10/23/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
| 10/23/2001 | 12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT) | 295LISTERIA | New England District Office (NWE-DO) |
| 10/23/2001 | 12AGP52CHEESE, SEMISOFT | 295LISTERIA | New England District Office (NWE-DO) |
Frequently Asked Questions
What is Dexpa's FDA import refusal history?
Dexpa (FEI: 1000603982) has 34 FDA import refusal record(s) in our database, spanning from 10/23/2001 to 11/19/2004.
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. Dexpa's FEI number is 1000603982.
What types of violations has Dexpa received?
Dexpa 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 Dexpa come from?
All FDA import refusal data for Dexpa 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.