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Dunci Sa

⚠️ Moderate Risk

FEI: 3000219048 • Guayaquil, Guayas • ECUADOR

FEI

FEI Number

3000219048

📍

Location

Guayaquil, Guayas

🇪🇨

Country

ECUADOR
🏢

Address

Unknown Street, , Guayaquil, Guayas, Ecuador

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/14/2006
Latest Refusal
6/14/2006
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
6/14/2006
16XGT21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
249FILTHY
New York District Office (NYK-DO)
6/14/2006
16XGT21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
249FILTHY
New York District Office (NYK-DO)
6/14/2006
16XGT21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
249FILTHY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Dunci Sa's FDA import refusal history?

Dunci Sa (FEI: 3000219048) has 3 FDA import refusal record(s) in our database, spanning from 6/14/2006 to 6/14/2006.

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. Dunci Sa's FEI number is 3000219048.

What types of violations has Dunci Sa received?

Dunci 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 Dunci Sa come from?

All FDA import refusal data for Dunci 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.