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ASOFARMA LABORATORIO

⚠️ High Risk

FEI: 3041025281 • Santa Fe • EL SALVADOR

FEI

FEI Number

3041025281

📍

Location

Santa Fe

🇸🇻
🏢

Address

Av Santa Fe 485, , Santa Fe, , El Salvador

High Risk

FDA Import Risk Assessment

52.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/8/2025
Latest Refusal
12/8/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
98.1×20%
Frequency
10.0×10%
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

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).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/8/2025
61LCB42RIVAROXABAN
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ASOFARMA LABORATORIO's FDA import refusal history?

ASOFARMA LABORATORIO (FEI: 3041025281) has 1 FDA import refusal record(s) in our database, spanning from 12/8/2025 to 12/8/2025.

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. ASOFARMA LABORATORIO's FEI number is 3041025281.

What types of violations has ASOFARMA LABORATORIO received?

ASOFARMA LABORATORIO has been cited for 2 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 ASOFARMA LABORATORIO come from?

All FDA import refusal data for ASOFARMA LABORATORIO 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.