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LABORATORIOS SUZIOS

⚠️ High Risk

FEI: 3017813851 • La Libertad • EL SALVADOR

FEI

FEI Number

3017813851

📍

Location

La Libertad

🇸🇻
🏢

Address

Carretera Puerto, , La Libertad, , El Salvador

High Risk

FDA Import Risk Assessment

59.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
3/7/2025
Latest Refusal
2/27/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
78.6×20%
Frequency
14.8×10%
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

753×

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
3/7/2025
60CDH09PHENYLEPHRINE HCL (ADRENERGIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/19/2023
54FGA99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/27/2023
64LCJ38HYDROCORTISONE ACETATE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LABORATORIOS SUZIOS's FDA import refusal history?

LABORATORIOS SUZIOS (FEI: 3017813851) has 3 FDA import refusal record(s) in our database, spanning from 2/27/2023 to 3/7/2025.

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. LABORATORIOS SUZIOS's FEI number is 3017813851.

What types of violations has LABORATORIOS SUZIOS received?

LABORATORIOS SUZIOS has been cited for 1 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 LABORATORIOS SUZIOS come from?

All FDA import refusal data for LABORATORIOS SUZIOS 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.