ImportRefusal LogoImportRefusal

Laboratorio Sued S.A

⚠️ Moderate Risk

FEI: 3005337453 • Santo Domingo De Guzman, Distrito Nacional • DOMINICAN REPUBLIC

FEI

FEI Number

3005337453

📍

Location

Santo Domingo De Guzman, Distrito Nacional

🇩🇴
🏢

Address

C/1 Era #5 Res Maria, , Santo Domingo De Guzman, Distrito Nacional, Dominican Republic

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
10/25/2005
Latest Refusal
10/25/2005
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

752×

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
10/25/2005
61WCA52TERBINAFINE HYDROCHLORIDE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/25/2005
61WCL52TERBINAFINE HYDROCHLORIDE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Laboratorio Sued S.A's FDA import refusal history?

Laboratorio Sued S.A (FEI: 3005337453) has 2 FDA import refusal record(s) in our database, spanning from 10/25/2005 to 10/25/2005.

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. Laboratorio Sued S.A's FEI number is 3005337453.

What types of violations has Laboratorio Sued S.A received?

Laboratorio Sued S.A 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 Laboratorio Sued S.A come from?

All FDA import refusal data for Laboratorio Sued S.A 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.