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Co. Corayma

⚠️ High Risk

FEI: 1000251506 • Presbiteriano • GUATEMALA

FEI

FEI Number

1000251506

📍

Location

Presbiteriano

🇬🇹

Country

GUATEMALA
🏢

Address

2176 Presbiteriano, , Presbiteriano, , Guatemala

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
8/22/2004
Latest Refusal
1/18/2004
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

2414×

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
8/22/2004
24AFC14STRINGBEANS
241PESTICIDE
New York District Office (NYK-DO)
8/22/2004
24AFC14STRINGBEANS
241PESTICIDE
New York District Office (NYK-DO)
6/22/2004
24AFC14STRINGBEANS
241PESTICIDE
New York District Office (NYK-DO)
1/18/2004
24AFC14STRINGBEANS
241PESTICIDE
New York District Office (NYK-DO)

Frequently Asked Questions

What is Co. Corayma's FDA import refusal history?

Co. Corayma (FEI: 1000251506) has 4 FDA import refusal record(s) in our database, spanning from 1/18/2004 to 8/22/2004.

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. Co. Corayma's FEI number is 1000251506.

What types of violations has Co. Corayma received?

Co. Corayma 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 Co. Corayma come from?

All FDA import refusal data for Co. Corayma 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.