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Gondi S.A.

⚠️ High Risk

FEI: 1000624023 • Portoviejo, Manabi • ECUADOR

FEI

FEI Number

1000624023

📍

Location

Portoviejo, Manabi

🇪🇨

Country

ECUADOR
🏢

Address

Km 5 1/2 Via Manta -Portoviejo, Conservas Ideal Plant (Industria De Enlatados Alimenticios Cia Ltda Ideal), Portoviejo, Manabi, Ecuador

High Risk

FDA Import Risk Assessment

63.0
LowModerateHighCritical

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

Statistics

17
Total Refusals
3
Unique Violations
4/26/2023
Latest Refusal
9/26/2002
Earliest Refusal

Score Breakdown

Violation Severity
97.7×40%
Refusal Volume
46.5×30%
Recency
45.8×20%
Frequency
8.3×10%
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

24913×

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.

3062×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

3082×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
4/26/2023
16AET33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
306INSANITARY
Division of Southeast Imports (DSEI)
4/26/2023
16AET33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
306INSANITARY
Division of Southeast Imports (DSEI)
8/31/2018
16AYT51MAHI MAHI
249FILTHY
Division of Southeast Imports (DSEI)
7/10/2018
16AEE33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
249FILTHY
Division of Northeast Imports (DNEI)
3/13/2012
16AGT51MAHI MAHI
249FILTHY
Florida District Office (FLA-DO)
6/9/2011
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
6/9/2011
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
6/9/2011
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
6/9/2011
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
6/9/2011
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
9/17/2008
16AGT51MAHI MAHI
249FILTHY
Florida District Office (FLA-DO)
11/4/2005
16AGC51MAHI MAHI
249FILTHY
Florida District Office (FLA-DO)
1/13/2003
16AGC51MAHI MAHI
249FILTHY
Florida District Office (FLA-DO)
1/13/2003
16AGC51MAHI MAHI
249FILTHY
Florida District Office (FLA-DO)
12/19/2002
16AGC51MAHI MAHI
308MFR INSAN
Florida District Office (FLA-DO)
12/19/2002
16AGC51MAHI MAHI
308MFR INSAN
Florida District Office (FLA-DO)
9/26/2002
16AGC45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
249FILTHY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

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

Gondi S.A. (FEI: 1000624023) has 17 FDA import refusal record(s) in our database, spanning from 9/26/2002 to 4/26/2023.

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. Gondi S.A.'s FEI number is 1000624023.

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

Gondi S.A. has been cited for 3 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 Gondi S.A. come from?

All FDA import refusal data for Gondi 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.