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FROMAGERIE BERTHAUT

⚠️ Moderate Risk

FEI: 3009871743 • Epoisses, Cote-d'Or • FRANCE

FEI

FEI Number

3009871743

📍

Location

Epoisses, Cote-d'Or

🇫🇷

Country

FRANCE
🏢

Address

Place du Champ De Foire, , Epoisses, Cote-d'Or, France

Moderate Risk

FDA Import Risk Assessment

35.6
LowModerateHighCritical

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

Statistics

20
Total Refusals
14
Unique Violations
12/2/2013
Latest Refusal
5/15/2003
Earliest Refusal

Score Breakdown

Violation Severity
47.6×40%
Refusal Volume
49.0×30%
Recency
0.0×20%
Frequency
18.9×10%
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

4829×

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.

3286×

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.

3246×

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)).

3216×

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.

2184×

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.

2954×

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.

3204×

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.

33204×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

3062×

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.

2562×

INCONSPICU

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)).

3081×

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.

20401×

SULFITELBL

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.

2811×

BACTERIA

The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains

111×

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).

Refusal History

DateProductViolationsDivision
12/2/2013
12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
324NO ENGLISH
Florida District Office (FLA-DO)
12/2/2013
12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
11UNSAFE COL
Florida District Office (FLA-DO)
7/25/2013
12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
218LIST INGRE
Division of Southeast Imports (DSEI)
9/21/2010
12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
256INCONSPICU
321LACKS N/C
324NO ENGLISH
3320TRANSFAT
482NUTRIT LBL
New England District Office (NWE-DO)
8/26/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
321LACKS N/C
324NO ENGLISH
New England District Office (NWE-DO)
8/26/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
218LIST INGRE
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)
8/26/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
218LIST INGRE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)
2/18/2010
12AFO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
Seattle District Office (SEA-DO)
2/18/2010
12AJO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
Seattle District Office (SEA-DO)
2/18/2010
12AJO56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
Seattle District Office (SEA-DO)
1/4/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
2040SULFITELBL
321LACKS N/C
324NO ENGLISH
328USUAL NAME
3320TRANSFAT
482NUTRIT LBL
New England District Office (NWE-DO)
1/4/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
328USUAL NAME
3320TRANSFAT
New England District Office (NWE-DO)
1/4/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
320LACKS FIRM
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)
1/4/2010
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
320LACKS FIRM
324NO ENGLISH
3320TRANSFAT
482NUTRIT LBL
New England District Office (NWE-DO)
1/4/2010
12AGT56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
256INCONSPICU
306INSANITARY
308MFR INSAN
324NO ENGLISH
482NUTRIT LBL
New England District Office (NWE-DO)
1/27/2009
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
306INSANITARY
Los Angeles District Office (LOS-DO)
1/26/2009
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
320LACKS FIRM
321LACKS N/C
328USUAL NAME
482NUTRIT LBL
New England District Office (NWE-DO)
3/17/2005
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
218LIST INGRE
482NUTRIT LBL
New York District Office (NYK-DO)
6/9/2003
12CGP15CHEESE, GOAT, N.E.C.
295LISTERIA
New York District Office (NYK-DO)
5/15/2003
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
281BACTERIA
New England District Office (NWE-DO)

Frequently Asked Questions

What is FROMAGERIE BERTHAUT's FDA import refusal history?

FROMAGERIE BERTHAUT (FEI: 3009871743) has 20 FDA import refusal record(s) in our database, spanning from 5/15/2003 to 12/2/2013.

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 BERTHAUT's FEI number is 3009871743.

What types of violations has FROMAGERIE BERTHAUT received?

FROMAGERIE BERTHAUT has been cited for 14 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 BERTHAUT come from?

All FDA import refusal data for FROMAGERIE BERTHAUT 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.