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Petrossian SA

⚠️ Moderate Risk

FEI: 3010012927 • Paris, Paris • FRANCE

FEI

FEI Number

3010012927

📍

Location

Paris, Paris

🇫🇷

Country

FRANCE
🏢

Address

18 boulevard de la Tour Maubourg, , Paris, Paris, France

Moderate Risk

FDA Import Risk Assessment

49.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/3/2003
Latest Refusal
4/22/2002
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
26.9×10%
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

2513×

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:

Refusal History

DateProductViolationsDivision
6/3/2003
16SGP42SWORDFISH, COLD SMOKED, FISH
251POISONOUS
New York District Office (NYK-DO)
1/14/2003
16SGP42SWORDFISH, COLD SMOKED, FISH
251POISONOUS
New York District Office (NYK-DO)
4/22/2002
16SGP42SWORDFISH, COLD SMOKED, FISH
251POISONOUS
New York District Office (NYK-DO)

Frequently Asked Questions

What is Petrossian SA's FDA import refusal history?

Petrossian SA (FEI: 3010012927) has 3 FDA import refusal record(s) in our database, spanning from 4/22/2002 to 6/3/2003.

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. Petrossian SA's FEI number is 3010012927.

What types of violations has Petrossian SA received?

Petrossian SA 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 Petrossian SA come from?

All FDA import refusal data for Petrossian 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.