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Jean Martin

⚠️ Moderate Risk

FEI: 3003163453 • Maussane Les Alpilles • FRANCE

FEI

FEI Number

3003163453

📍

Location

Maussane Les Alpilles

🇫🇷

Country

FRANCE
🏢

Address

Rue Charloun Rieu, B.P. 1, Maussane Les Alpilles, , France

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/8/2001
Latest Refusal
11/8/2001
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

831×

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.

Refusal History

DateProductViolationsDivision
11/8/2001
25HCE99MIXED VEGETABLES, WITH SAUCE, N.E.C.
83NO PROCESS
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Jean Martin's FDA import refusal history?

Jean Martin (FEI: 3003163453) has 1 FDA import refusal record(s) in our database, spanning from 11/8/2001 to 11/8/2001.

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. Jean Martin's FEI number is 3003163453.

What types of violations has Jean Martin received?

Jean Martin has been cited for 1 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 Jean Martin come from?

All FDA import refusal data for Jean Martin 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.