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Borde SA

⚠️ Moderate Risk

FEI: 3002809317 • Saugues • FRANCE

FEI

FEI Number

3002809317

📍

Location

Saugues

🇫🇷

Country

FRANCE
🏢

Address

Les Gardelles, , Saugues, , France

Moderate Risk

FDA Import Risk Assessment

45.4
LowModerateHighCritical

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

Statistics

23
Total Refusals
10
Unique Violations
5/19/2017
Latest Refusal
9/18/2003
Earliest Refusal

Score Breakdown

Violation Severity
70.9×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
16.8×10%
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

24912×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

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.

4734×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

20402×

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.

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)).

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

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:

2971×

AFLATOXIN

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

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
5/19/2017
25QGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C.
249FILTHY
Division of West Coast Imports (DWCI)
1/26/2012
25RHH99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
2040SULFITELBL
New York District Office (NYK-DO)
1/26/2012
25RHH99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
2040SULFITELBL
New York District Office (NYK-DO)
3/4/2010
25QGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C.
238UNSAFE ADD
249FILTHY
Philadelphia District Office (PHI-DO)
12/30/2009
25PGH07MUSHROOM, CHANTERELLE, WHOLE (BUTTON) (FUNGI)
249FILTHY
New York District Office (NYK-DO)
12/16/2009
25QGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, PIECES AND STEMS, SLICED, N.E.C.
249FILTHY
Southwest Import District Office (SWI-DO)
10/13/2009
25PGH07MUSHROOM, CHANTERELLE, WHOLE (BUTTON) (FUNGI)
249FILTHY
New York District Office (NYK-DO)
4/22/2009
25SGR03MUSHROOM, STRAW, FUNGI PRODUCTS, N.E.C.
249FILTHY
New York District Office (NYK-DO)
10/4/2006
25RGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
249FILTHY
320LACKS FIRM
Florida District Office (FLA-DO)
10/4/2006
25RGH07MUSHROOM, CHANTERELLE, BROKEN OR KIBBLED
249FILTHY
Florida District Office (FLA-DO)
10/4/2006
25RCT07MUSHROOM, CHANTERELLE, BROKEN OR KIBBLED
83NO PROCESS
Florida District Office (FLA-DO)
10/4/2006
25RCT06MUSHROOM, MOREL, BROKEN OR KIBBLED
83NO PROCESS
Florida District Office (FLA-DO)
10/31/2004
25RGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
249FILTHY
New York District Office (NYK-DO)
7/16/2004
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
Florida District Office (FLA-DO)
5/24/2004
25PGH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
Florida District Office (FLA-DO)
3/24/2004
20AET05CURRANTS, BLACK (BERRY)
473LABELING
482NUTRIT LBL
Atlanta District Office (ATL-DO)
3/24/2004
20AET04CRANBERRIES (BERRY)
473LABELING
482NUTRIT LBL
Atlanta District Office (ATL-DO)
3/24/2004
20AET14STRAWBERRIES (BERRY)
473LABELING
482NUTRIT LBL
Atlanta District Office (ATL-DO)
3/24/2004
21GET03CHERRY FRUIT (PIT FRUIT)
473LABELING
482NUTRIT LBL
Atlanta District Office (ATL-DO)
3/24/2004
25QEI07MUSHROOM, CHANTERELLE, PIECES AND STEMS, SLICED
324NO ENGLISH
482NUTRIT LBL
Atlanta District Office (ATL-DO)
1/5/2004
25PGH06MUSHROOM, MOREL, WHOLE (BUTTON) (FUNGI)
297AFLATOXIN
Atlanta District Office (ATL-DO)
9/24/2003
25PGH06MUSHROOM, MOREL, WHOLE (BUTTON) (FUNGI)
251POISONOUS
324NO ENGLISH
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
9/18/2003
25PCE99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Borde SA's FDA import refusal history?

Borde SA (FEI: 3002809317) has 23 FDA import refusal record(s) in our database, spanning from 9/18/2003 to 5/19/2017.

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. Borde SA's FEI number is 3002809317.

What types of violations has Borde SA received?

Borde SA has been cited for 10 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 Borde SA come from?

All FDA import refusal data for Borde SA 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.