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TROPIX S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3004262981 • Sacacoyo, La Libertad • EL SALVADOR

FEI

FEI Number

3004262981

📍

Location

Sacacoyo, La Libertad

🇸🇻
🏢

Address

Calle La Guadalupana No.4, Caserio El Tigre. Ateos, , Sacacoyo, La Libertad, El Salvador

Moderate Risk

FDA Import Risk Assessment

39.6
LowModerateHighCritical

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

Statistics

8
Total Refusals
6
Unique Violations
1/20/2015
Latest Refusal
3/5/2009
Earliest Refusal

Score Breakdown

Violation Severity
69.0×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
13.6×10%
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

4823×

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.

2492×

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.

92×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

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.

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
1/20/2015
37JGT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
482NUTRIT LBL
Division of Southeast Imports (DSEI)
1/20/2015
37JGT08TOMATO SAUCE (WITH OTHER INGREDIENTS)
482NUTRIT LBL
Division of Southeast Imports (DSEI)
2/4/2014
05BGT99BREAKFAST FOOD QUICK OR INSTANT COOKING, N.E.C.
11UNSAFE COL
Los Angeles District Office (LOS-DO)
2/3/2014
23KGT01PUMPKIN SEED (EDIBLE SEED)
9SALMONELLA
Los Angeles District Office (LOS-DO)
1/30/2014
02BGT02CORN, PLAIN MEAL
249FILTHY
Philadelphia District Office (PHI-DO)
12/26/2013
02BYY02CORN, PLAIN MEAL
249FILTHY
Philadelphia District Office (PHI-DO)
1/10/2012
30FGT99BEVERAGE BASE OF NON-FRUIT ORIGIN, N.E.C.
218LIST INGRE
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
3/5/2009
28KHT99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C.
9SALMONELLA
New York District Office (NYK-DO)

Frequently Asked Questions

What is TROPIX S.A. DE C.V.'s FDA import refusal history?

TROPIX S.A. DE C.V. (FEI: 3004262981) has 8 FDA import refusal record(s) in our database, spanning from 3/5/2009 to 1/20/2015.

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. TROPIX S.A. DE C.V.'s FEI number is 3004262981.

What types of violations has TROPIX S.A. DE C.V. received?

TROPIX S.A. DE C.V. has been cited for 6 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 TROPIX S.A. DE C.V. come from?

All FDA import refusal data for TROPIX S.A. DE C.V. 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.