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Artico S.A.

⚠️ High Risk

FEI: 3003002494 • Rio Grande, Rio Grande do sul • BRAZIL

FEI

FEI Number

3003002494

📍

Location

Rio Grande, Rio Grande do sul

🇧🇷

Country

BRAZIL
🏢

Address

Rua Forte Santana, 67 69, , Rio Grande, Rio Grande do sul, Brazil

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
6/4/2013
Latest Refusal
9/7/2012
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

94×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
6/4/2013
16AGT13CROAKER
9SALMONELLA
New York District Office (NYK-DO)
6/4/2013
16AGT13CROAKER
9SALMONELLA
New York District Office (NYK-DO)
6/4/2013
16AGT13CROAKER
9SALMONELLA
New York District Office (NYK-DO)
9/7/2012
16AGD13CROAKER
9SALMONELLA
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Artico S.A.'s FDA import refusal history?

Artico S.A. (FEI: 3003002494) has 4 FDA import refusal record(s) in our database, spanning from 9/7/2012 to 6/4/2013.

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. Artico S.A.'s FEI number is 3003002494.

What types of violations has Artico S.A. received?

Artico S.A. 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 Artico S.A. come from?

All FDA import refusal data for Artico S.A. 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.