ImportRefusal LogoImportRefusal

NUEVA EPS

⚠️ Moderate Risk

FEI: 3014550485 • Bogota, Cundinamarca • COLOMBIA

FEI

FEI Number

3014550485

📍

Location

Bogota, Cundinamarca

🇨🇴

Country

COLOMBIA
🏢

Address

Carrera 85l No. 46a-66 Piso 2, , Bogota, Cundinamarca, Colombia

Moderate Risk

FDA Import Risk Assessment

41.6
LowModerateHighCritical

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

Statistics

5
Total Refusals
2
Unique Violations
7/31/2018
Latest Refusal
7/31/2018
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

1185×

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).

755×

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
7/31/2018
60LDY05ASPIRIN (ANALGESIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/31/2018
60XDY02METOPROLOL (ANTI-ADRENERGIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/31/2018
62ODY41LOSARTAN POTASSIUM (ANTI-HYPERTENSIVE - PART II)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/31/2018
61TDY29SCOPOLAMINE (ANTI-EMETIC/NAUSEANT)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/31/2018
61MDY25PRIMIDONE (ANTI-CONVULSANT)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NUEVA EPS's FDA import refusal history?

NUEVA EPS (FEI: 3014550485) has 5 FDA import refusal record(s) in our database, spanning from 7/31/2018 to 7/31/2018.

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. NUEVA EPS's FEI number is 3014550485.

What types of violations has NUEVA EPS received?

NUEVA EPS 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 NUEVA EPS come from?

All FDA import refusal data for NUEVA EPS 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.