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Corporation Arso, S. A. (Factory 2)

⚠️ Moderate Risk

FEI: 3005258310 • San Marcos, San Marcos • GUATEMALA

FEI

FEI Number

3005258310

📍

Location

San Marcos, San Marcos

🇬🇹

Country

GUATEMALA
🏢

Address

Aldea San Jeronimo, Tumbador, San Marcos, San Marcos, Guatemala

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/24/2010
Latest Refusal
11/24/2010
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
11/24/2010
21SFB17RAMBUTAN (SUBTROPICAL AND TROPICAL FRUIT)
241PESTICIDE
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Corporation Arso, S. A. (Factory 2)'s FDA import refusal history?

Corporation Arso, S. A. (Factory 2) (FEI: 3005258310) has 1 FDA import refusal record(s) in our database, spanning from 11/24/2010 to 11/24/2010.

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. Corporation Arso, S. A. (Factory 2)'s FEI number is 3005258310.

What types of violations has Corporation Arso, S. A. (Factory 2) received?

Corporation Arso, S. A. (Factory 2) 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 Corporation Arso, S. A. (Factory 2) come from?

All FDA import refusal data for Corporation Arso, S. A. (Factory 2) 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.