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PLASSE SA

⚠️ High Risk

FEI: 3004307282 • Jassans Riottier, AIN • FRANCE

FEI

FEI Number

3004307282

📍

Location

Jassans Riottier, AIN

🇫🇷

Country

FRANCE
🏢

Address

766 Rue Edouard Herriot, , Jassans Riottier, AIN, France

High Risk

FDA Import Risk Assessment

63.3
LowModerateHighCritical

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

Statistics

28
Total Refusals
6
Unique Violations
9/9/2004
Latest Refusal
10/3/2001
Earliest Refusal

Score Breakdown

Violation Severity
93.7×40%
Refusal Volume
54.2×30%
Recency
0.0×20%
Frequency
95.3×10%
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

29524×

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.

2812×

BACTERIA

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

2181×

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.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

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.

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.

Refusal History

DateProductViolationsDivision
9/9/2004
12CFP15CHEESE, GOAT, N.E.C.
295LISTERIA
San Francisco District Office (SAN-DO)
9/9/2004
12CFP15CHEESE, GOAT, N.E.C.
295LISTERIA
San Francisco District Office (SAN-DO)
9/9/2004
12CFP15CHEESE, GOAT, N.E.C.
295LISTERIA
San Francisco District Office (SAN-DO)
9/9/2004
12AFP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
San Francisco District Office (SAN-DO)
9/9/2004
12AFP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
San Francisco District Office (SAN-DO)
5/15/2003
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
New England District Office (NWE-DO)
5/15/2003
12AGP52CHEESE, SEMISOFT
281BACTERIA
New England District Office (NWE-DO)
5/15/2003
12AGP52CHEESE, SEMISOFT
281BACTERIA
New England District Office (NWE-DO)
5/15/2003
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
218LIST INGRE
260FALSE
321LACKS N/C
New England District Office (NWE-DO)
4/22/2002
12AFP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
308MFR INSAN
San Francisco District Office (SAN-DO)
2/20/2002
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
2/20/2002
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
New England District Office (NWE-DO)
1/23/2002
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
1/23/2002
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
12/26/2001
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
New England District Office (NWE-DO)
12/26/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
12/26/2001
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)
11/20/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
11/20/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
11/8/2001
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
New England District Office (NWE-DO)
11/8/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/23/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/23/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/23/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/3/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/3/2001
12AGP52CHEESE, SEMISOFT
295LISTERIA
New England District Office (NWE-DO)
10/3/2001
12AGP56SOFT RIPENED CHEESE MADE FROM COW'S MILK (E.G., BRIE, CAMEMBERT)
295LISTERIA
New England District Office (NWE-DO)

Frequently Asked Questions

What is PLASSE SA's FDA import refusal history?

PLASSE SA (FEI: 3004307282) has 28 FDA import refusal record(s) in our database, spanning from 10/3/2001 to 9/9/2004.

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. PLASSE SA's FEI number is 3004307282.

What types of violations has PLASSE SA received?

PLASSE SA has been cited for 6 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 PLASSE SA come from?

All FDA import refusal data for PLASSE 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.