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FROMAGERIE BOUCHET

⚠️ Moderate Risk

FEI: 3004293290 • Beaumont, Haute Savoie • FRANCE

FEI

FEI Number

3004293290

📍

Location

Beaumont, Haute Savoie

🇫🇷

Country

FRANCE
🏢

Address

Zone D Activite Juge Guerin, , Beaumont, Haute Savoie, France

Moderate Risk

FDA Import Risk Assessment

46.4
LowModerateHighCritical

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

Statistics

8
Total Refusals
4
Unique Violations
4/20/2011
Latest Refusal
1/26/2004
Earliest Refusal

Score Breakdown

Violation Severity
86.7×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
11.1×10%
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

3086×

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.

3063×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

2952×

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.

3241×

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)).

Refusal History

DateProductViolationsDivision
4/20/2011
12AGP19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
306INSANITARY
308MFR INSAN
New York District Office (NYK-DO)
1/20/2011
12AGO52CHEESE, SEMISOFT
306INSANITARY
308MFR INSAN
New York District Office (NYK-DO)
9/29/2010
12AGO52CHEESE, SEMISOFT
306INSANITARY
308MFR INSAN
New York District Office (NYK-DO)
11/29/2005
12AGP99CHEESE (STANDARDIZED),N.E.C.
308MFR INSAN
New York District Office (NYK-DO)
2/14/2005
12AGP52CHEESE, SEMISOFT
308MFR INSAN
New York District Office (NYK-DO)
1/31/2005
12AGP52CHEESE, SEMISOFT
295LISTERIA
New York District Office (NYK-DO)
8/19/2004
12AGP52CHEESE, SEMISOFT
295LISTERIA
New York District Office (NYK-DO)
1/26/2004
12AGP52CHEESE, SEMISOFT
308MFR INSAN
324NO ENGLISH
New York District Office (NYK-DO)

Frequently Asked Questions

What is FROMAGERIE BOUCHET's FDA import refusal history?

FROMAGERIE BOUCHET (FEI: 3004293290) has 8 FDA import refusal record(s) in our database, spanning from 1/26/2004 to 4/20/2011.

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 BOUCHET's FEI number is 3004293290.

What types of violations has FROMAGERIE BOUCHET received?

FROMAGERIE BOUCHET has been cited for 4 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 BOUCHET come from?

All FDA import refusal data for FROMAGERIE BOUCHET 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.