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Zeneida Altamirano

⚠️ Moderate Risk

FEI: 3001634067 • Managua, Managua • NICARAGUA

FEI

FEI Number

3001634067

📍

Location

Managua, Managua

🇳🇮

Country

NICARAGUA
🏢

Address

Villa Floor Sur 5ta Calle No 190, , Managua, Managua, Nicaragua

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

6
Total Refusals
3
Unique Violations
7/21/2008
Latest Refusal
6/19/2002
Earliest Refusal

Score Breakdown

Violation Severity
48.3×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
9.8×10%
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

4734×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2491×

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
7/21/2008
07AGT99BAKED SNACK FOOD, N.E.C.
473LABELING
Florida District Office (FLA-DO)
7/18/2008
21UGT99SUBTROPICAL AND TROPICAL FRUIT, JAM, JELLY, PRESERVES, MARMALADE, BUTTER OR CANDIED, N.E.C.
473LABELING
Florida District Office (FLA-DO)
7/18/2008
33JGT02CARAMEL CANDY PIECES, SOFT, WITH FRUIT (WITHOUT CHOCOLATE)
473LABELING
Florida District Office (FLA-DO)
7/18/2008
33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE)
473LABELING
Florida District Office (FLA-DO)
6/10/2008
21XGC14TAMARIND (SUBTROPICAL/TROPICAL FRUIT PULP)
249FILTHY
Florida District Office (FLA-DO)
6/19/2002
05AGT01CORN FLAKES,PUFFS,KRISPIES,LOOPS READY TO EAT
324NO ENGLISH
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Zeneida Altamirano's FDA import refusal history?

Zeneida Altamirano (FEI: 3001634067) has 6 FDA import refusal record(s) in our database, spanning from 6/19/2002 to 7/21/2008.

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. Zeneida Altamirano's FEI number is 3001634067.

What types of violations has Zeneida Altamirano received?

Zeneida Altamirano 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 Zeneida Altamirano come from?

All FDA import refusal data for Zeneida Altamirano 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.