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Steiner, S.A. de C.V.

⚠️ High Risk

FEI: 3010105725 • Antiguo Cuscatlan, La Libertad • EL SALVADOR

FEI

FEI Number

3010105725

📍

Location

Antiguo Cuscatlan, La Libertad

🇸🇻
🏢

Address

Calle Siemens bodega No. 65, Zona Industrial Santa Elena, Antiguo Cuscatlan, La Libertad, El Salvador

High Risk

FDA Import Risk Assessment

57.0
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
12/14/2025
Latest Refusal
12/7/2015
Earliest Refusal

Score Breakdown

Violation Severity
68.3×40%
Refusal Volume
31.3×30%
Recency
98.6×20%
Frequency
6.0×10%
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

833×

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.

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

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)).

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.

Refusal History

DateProductViolationsDivision
12/14/2025
37JGI07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Division of Northeast Imports (DNEI)
12/14/2025
37JGI07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Division of Northeast Imports (DNEI)
12/14/2025
37JGI07STEAK AND OTHER MEAT SAUCE
83NO PROCESS
Division of Northeast Imports (DNEI)
11/8/2022
02CFT01RICE FLOUR
241PESTICIDE
Division of Northeast Imports (DNEI)
5/5/2022
04BGT02NOODLES, EGG
324NO ENGLISH
Division of Northern Border Imports (DNBI)
12/7/2015
04CFT01NOODLES, CHOW MEIN
482NUTRIT LBL
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Steiner, S.A. de C.V.'s FDA import refusal history?

Steiner, S.A. de C.V. (FEI: 3010105725) has 6 FDA import refusal record(s) in our database, spanning from 12/7/2015 to 12/14/2025.

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. Steiner, S.A. de C.V.'s FEI number is 3010105725.

What types of violations has Steiner, S.A. de C.V. received?

Steiner, S.A. de C.V. 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 Steiner, S.A. de C.V. come from?

All FDA import refusal data for Steiner, 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.