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Mardex, S.A.

⚠️ High Risk

FEI: 3002808738 • Manta, Manabi • ECUADOR

FEI

FEI Number

3002808738

📍

Location

Manta, Manabi

🇪🇨

Country

ECUADOR
🏢

Address

Avenida 102, Calle 124 Los Esteros, , Manta, Manabi, Ecuador

High Risk

FDA Import Risk Assessment

53.1
LowModerateHighCritical

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

Statistics

22
Total Refusals
4
Unique Violations
11/30/2018
Latest Refusal
1/24/2003
Earliest Refusal

Score Breakdown

Violation Severity
91.5×40%
Refusal Volume
50.4×30%
Recency
0.0×20%
Frequency
13.9×10%
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

24921×

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.

2603×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

38781×

POISONORD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:

Refusal History

DateProductViolationsDivision
11/30/2018
16AVC51MAHI MAHI
3878POISONORD
Division of Southeast Imports (DSEI)
7/19/2018
16AVT51MAHI MAHI
249FILTHY
Division of Northeast Imports (DNEI)
7/19/2018
16AVT51MAHI MAHI
249FILTHY
Division of Northeast Imports (DNEI)
7/12/2016
16AVT51MAHI MAHI
249FILTHY
Baltimore District Office (BLT-DO)
7/12/2016
16AVT51MAHI MAHI
249FILTHY
Baltimore District Office (BLT-DO)
7/12/2016
16AVT51MAHI MAHI
249FILTHY
Baltimore District Office (BLT-DO)
7/12/2016
16AVT51MAHI MAHI
249FILTHY
Baltimore District Office (BLT-DO)
8/1/2011
16AVT35SHARK
249FILTHY
New York District Office (NYK-DO)
8/1/2011
16AVT35SHARK
249FILTHY
New York District Office (NYK-DO)
2/16/2010
16AGT51MAHI MAHI
249FILTHY
260FALSE
320LACKS FIRM
Florida District Office (FLA-DO)
2/16/2010
16AGT51MAHI MAHI
249FILTHY
260FALSE
Florida District Office (FLA-DO)
2/16/2010
16AGT51MAHI MAHI
249FILTHY
260FALSE
Florida District Office (FLA-DO)
9/7/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
7/16/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
7/16/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
7/16/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
7/16/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
7/16/2007
16AGD51MAHI MAHI
249FILTHY
Seattle District Office (SEA-DO)
2/14/2006
16AFD51MAHI MAHI
249FILTHY
New York District Office (NYK-DO)
2/25/2004
16AGD51MAHI MAHI
249FILTHY
New York District Office (NYK-DO)
1/24/2003
16AGT54MARLIN
249FILTHY
Florida District Office (FLA-DO)
1/24/2003
16AGT17GROUPERS
249FILTHY
Florida District Office (FLA-DO)

Frequently Asked Questions

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

Mardex, S.A. (FEI: 3002808738) has 22 FDA import refusal record(s) in our database, spanning from 1/24/2003 to 11/30/2018.

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. Mardex, S.A.'s FEI number is 3002808738.

What types of violations has Mardex, S.A. received?

Mardex, S.A. has been cited for 4 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 Mardex, S.A. come from?

All FDA import refusal data for Mardex, 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.