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PROLAIDIS

⚠️ High Risk

FEI: 2000045406 • Lesquin, Nord • FRANCE

FEI

FEI Number

2000045406

📍

Location

Lesquin, Nord

🇫🇷

Country

FRANCE
🏢

Address

69 rue de la Croix Bougard, , Lesquin, Nord, France

High Risk

FDA Import Risk Assessment

61.6
LowModerateHighCritical

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

Statistics

15
Total Refusals
2
Unique Violations
9/4/2013
Latest Refusal
5/2/2013
Earliest Refusal

Score Breakdown

Violation Severity
95.6×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

24915×

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.

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
9/4/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
Division of Northeast Imports (DNEI)
8/5/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
Division of Northeast Imports (DNEI)
7/25/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
7/25/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
7/8/2013
12AGO52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
6/7/2013
12AGP19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
249FILTHY
324NO ENGLISH
New York District Office (NYK-DO)
6/3/2013
12AGO52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
5/30/2013
12AFD19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
249FILTHY
New York District Office (NYK-DO)
5/30/2013
12AGP19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
249FILTHY
New York District Office (NYK-DO)
5/22/2013
12AGO52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
5/16/2013
12AGP19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
249FILTHY
New York District Office (NYK-DO)
5/16/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
5/16/2013
12AGP52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)
5/2/2013
12AGP19CHEESE, HARD (CHESIRE,ESRUM,FORTINA,FORTINE,KASSENI,MOZZARELLA,MONTASIO,PECARINO,PORT SALUT, ETC)
249FILTHY
New York District Office (NYK-DO)
5/2/2013
12AGO52CHEESE, SEMISOFT
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is PROLAIDIS's FDA import refusal history?

PROLAIDIS (FEI: 2000045406) has 15 FDA import refusal record(s) in our database, spanning from 5/2/2013 to 9/4/2013.

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. PROLAIDIS's FEI number is 2000045406.

What types of violations has PROLAIDIS received?

PROLAIDIS has been cited for 2 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 PROLAIDIS come from?

All FDA import refusal data for PROLAIDIS 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.