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Comercializadora Mar Azul Export Ca

⚠️ High Risk

FEI: 3005770681 • Caracas • VENEZUELA

FEI

FEI Number

3005770681

📍

Location

Caracas

🇻🇪

Country

VENEZUELA
🏢

Address

Ka Canada De Urdaneta, Local 2, Caracas, , Venezuela

High Risk

FDA Import Risk Assessment

51.5
LowModerateHighCritical

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

Statistics

10
Total Refusals
2
Unique Violations
7/16/2010
Latest Refusal
11/30/2006
Earliest Refusal

Score Breakdown

Violation Severity
93.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
27.6×10%
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

2499×

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.

3241×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

Refusal History

DateProductViolationsDivision
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
7/16/2010
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
10/22/2009
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
10/22/2009
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
9/17/2009
16JGN01CRAB
249FILTHY
Florida District Office (FLA-DO)
11/30/2006
16JGN01CRAB
324NO ENGLISH
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Comercializadora Mar Azul Export Ca's FDA import refusal history?

Comercializadora Mar Azul Export Ca (FEI: 3005770681) has 10 FDA import refusal record(s) in our database, spanning from 11/30/2006 to 7/16/2010.

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. Comercializadora Mar Azul Export Ca's FEI number is 3005770681.

What types of violations has Comercializadora Mar Azul Export Ca received?

Comercializadora Mar Azul Export Ca has been cited for 2 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 Comercializadora Mar Azul Export Ca come from?

All FDA import refusal data for Comercializadora Mar Azul Export Ca 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.