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Dexpa

⚠️ High Risk

FEI: 1000603982 • Thiais, Val de Marne • FRANCE

FEI

FEI Number

1000603982

📍

Location

Thiais, Val de Marne

🇫🇷

Country

FRANCE
🏢

Address

5 Rue Des Hauts Flouviers, , Thiais, Val de Marne, France

High Risk

FDA Import Risk Assessment

56.2
LowModerateHighCritical

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

Statistics

34
Total Refusals
8
Unique Violations
11/19/2004
Latest Refusal
10/23/2001
Earliest Refusal

Score Breakdown

Violation Severity
72.5×40%
Refusal Volume
57.2×30%
Recency
0.0×20%
Frequency
100.0×10%
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

29527×

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.

32410×

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)).

4826×

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.

2511×

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:

3281×

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.

3211×

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.

2531×

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.

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.

Refusal History

DateProductViolationsDivision
11/19/2004
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
324NO ENGLISH
New England District Office (NWE-DO)
11/19/2004
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
324NO ENGLISH
New England District Office (NWE-DO)
11/19/2004
12AHP99CHEESE (STANDARDIZED),N.E.C.
295LISTERIA
324NO ENGLISH
New England District Office (NWE-DO)
11/19/2004
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
324NO ENGLISH
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)
324NO ENGLISH
482NUTRIT LBL
New England District Office (NWE-DO)
4/1/2004
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
251POISONOUS
324NO ENGLISH
482NUTRIT LBL
New England District Office (NWE-DO)
12/16/2003
12AGP16CHEESE, GOUDA
324NO ENGLISH
New England District Office (NWE-DO)
12/16/2003
12AGP52CHEESE, SEMISOFT
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)
6/9/2003
12AGP52CHEESE, SEMISOFT
324NO ENGLISH
482NUTRIT LBL
New York District Office (NYK-DO)
6/9/2003
12AGP52CHEESE, SEMISOFT
324NO ENGLISH
482NUTRIT LBL
New York District Office (NYK-DO)
6/9/2003
12AGP52CHEESE, SEMISOFT
253STD IDENT
324NO ENGLISH
482NUTRIT LBL
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.