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Productos Nica Oscar Santana

⚠️ Moderate Risk

FEI: 3005078229 • Managua, NI-MN • NICARAGUA

FEI

FEI Number

3005078229

📍

Location

Managua, NI-MN

🇳🇮

Country

NICARAGUA
🏢

Address

Mercado Roberto Huembes Modulo b- 9, , Managua, NI-MN, Nicaragua

Moderate Risk

FDA Import Risk Assessment

44.7
LowModerateHighCritical

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

Statistics

14
Total Refusals
10
Unique Violations
8/3/2022
Latest Refusal
11/13/2006
Earliest Refusal

Score Breakdown

Violation Severity
61.2×40%
Refusal Volume
43.6×30%
Recency
31.2×20%
Frequency
8.9×10%
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

4735×

LABELING

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

2814×

BACTERIA

The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

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)).

38651×

COLORLABEL

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.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

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.

Refusal History

DateProductViolationsDivision
8/3/2022
03RGT35PASTRY, FRUIT OR JELLY FILLED, WITHOUT CUSTARD OR CREAM FILLING
249FILTHY
Division of Southeast Imports (DSEI)
3/20/2017
50CGT01ANNATO SEEDS FOR COLOR MANUFACTURING
3865COLORLABEL
Division of Southeast Imports (DSEI)
3/20/2017
30FCT01BEVERAGE BASE, COLA
473LABELING
Division of Southeast Imports (DSEI)
3/20/2017
28AMD13CINNAMON, CASSIA, WHOLE (SPICE)
473LABELING
Division of Southeast Imports (DSEI)
3/20/2017
34HGT03COCOA DAIRY MIX
473LABELING
Division of Southeast Imports (DSEI)
3/20/2017
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
473LABELING
Division of Southeast Imports (DSEI)
3/20/2017
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
473LABELING
Division of Southeast Imports (DSEI)
3/20/2017
16AET33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
281BACTERIA
Division of Southeast Imports (DSEI)
3/20/2017
23YGT99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C.
281BACTERIA
Division of Southeast Imports (DSEI)
3/20/2017
31AYY02COFFEE, GROUND
281BACTERIA
Division of Southeast Imports (DSEI)
3/20/2017
12CGB99CHEESE PRODUCTS, NON-STANDARDIZED, N.E.C.
281BACTERIA
Division of Southeast Imports (DSEI)
2/15/2007
02GGT01BARLEY FLOUR
274COLOR LBLG
324NO ENGLISH
Florida District Office (FLA-DO)
2/15/2007
28JGT99MIXED SPICES AND SEASONING WITH SALT, N.E.C.
62NEEDS FCE
83NO PROCESS
Florida District Office (FLA-DO)
11/13/2006
30FCT01BEVERAGE BASE, COLA
218LIST INGRE
482NUTRIT LBL
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Productos Nica Oscar Santana's FDA import refusal history?

Productos Nica Oscar Santana (FEI: 3005078229) has 14 FDA import refusal record(s) in our database, spanning from 11/13/2006 to 8/3/2022.

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. Productos Nica Oscar Santana's FEI number is 3005078229.

What types of violations has Productos Nica Oscar Santana received?

Productos Nica Oscar Santana has been cited for 10 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 Productos Nica Oscar Santana come from?

All FDA import refusal data for Productos Nica Oscar Santana 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.