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Fromagerie Pujol Et Coundray

⚠️ Moderate Risk

FEI: 3003652356 • Moulis, Ariege • FRANCE

FEI

FEI Number

3003652356

📍

Location

Moulis, Ariege

🇫🇷

Country

FRANCE
🏢

Address

Unknown Street, , Moulis, Ariege, France

Moderate Risk

FDA Import Risk Assessment

35.9
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
3
Unique Violations
7/1/2014
Latest Refusal
8/18/2005
Earliest Refusal

Score Breakdown

Violation Severity
66.7×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
5.6×10%
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

2953×

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.

3242×

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)).

4821×

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.

Refusal History

DateProductViolationsDivision
7/1/2014
12AGP52CHEESE, SEMISOFT
324NO ENGLISH
482NUTRIT LBL
New York District Office (NYK-DO)
12/10/2013
12AGO64SOFT RIPENED CHEESE MADE FROM A MIXTURE OF ANIMAL MILK
295LISTERIA
New York District Office (NYK-DO)
1/8/2009
12AFP52CHEESE, SEMISOFT
324NO ENGLISH
Los Angeles District Office (LOS-DO)
10/18/2007
12CGP15CHEESE, GOAT, N.E.C.
295LISTERIA
New York District Office (NYK-DO)
8/18/2005
12AFP52CHEESE, SEMISOFT
295LISTERIA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Fromagerie Pujol Et Coundray's FDA import refusal history?

Fromagerie Pujol Et Coundray (FEI: 3003652356) has 5 FDA import refusal record(s) in our database, spanning from 8/18/2005 to 7/1/2014.

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. Fromagerie Pujol Et Coundray's FEI number is 3003652356.

What types of violations has Fromagerie Pujol Et Coundray received?

Fromagerie Pujol Et Coundray has been cited for 3 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 Fromagerie Pujol Et Coundray come from?

All FDA import refusal data for Fromagerie Pujol Et Coundray 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.