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Sistemas Medicos ALARIS SA de CV

⚠️ Moderate Risk

FEI: 3002808169 • Tijuana, Baja California Norte • MEXICO

FEI

FEI Number

3002808169

📍

Location

Tijuana, Baja California Norte

🇲🇽

Country

MEXICO
🏢

Address

Blvd. Insurgentes # 20351, Parque Industrial El Florido seccion Vistas 1, Tijuana, Baja California Norte, Mexico

Moderate Risk

FDA Import Risk Assessment

41.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
4/8/2025
Latest Refusal
5/8/2017
Earliest Refusal

Score Breakdown

Violation Severity
54.0×40%
Refusal Volume
17.7×30%
Recency
69.6×20%
Frequency
2.5×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4791×

DV QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
4/8/2025
80FPASET, ADMINISTRATION, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
5/8/2017
80FPASET, ADMINISTRATION, INTRAVASCULAR
479DV QUALITY
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Sistemas Medicos ALARIS SA de CV's FDA import refusal history?

Sistemas Medicos ALARIS SA de CV (FEI: 3002808169) has 2 FDA import refusal record(s) in our database, spanning from 5/8/2017 to 4/8/2025.

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. Sistemas Medicos ALARIS SA de CV's FEI number is 3002808169.

What types of violations has Sistemas Medicos ALARIS SA de CV received?

Sistemas Medicos ALARIS SA de CV has been cited for 5 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 Sistemas Medicos ALARIS SA de CV come from?

All FDA import refusal data for Sistemas Medicos ALARIS SA de CV 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.