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YURANY ANDREA JIMENEZ MUNOZ

⚠️ Moderate Risk

FEI: 3014241760 • Medellin, Antioquia • COLOMBIA

FEI

FEI Number

3014241760

📍

Location

Medellin, Antioquia

🇨🇴

Country

COLOMBIA
🏢

Address

Deprisa -Logistica Internacional, Cra 80 B 40- 11 Apto 402 Laur, Medellin, Antioquia, Colombia

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
3/14/2018
Latest Refusal
3/14/2018
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
3/14/2018
62KCB10OMEPRAZOLE (ANTI-PERISTALTIC, ANTI-DIARRHEAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/14/2018
62ODB14AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is YURANY ANDREA JIMENEZ MUNOZ's FDA import refusal history?

YURANY ANDREA JIMENEZ MUNOZ (FEI: 3014241760) has 2 FDA import refusal record(s) in our database, spanning from 3/14/2018 to 3/14/2018.

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. YURANY ANDREA JIMENEZ MUNOZ's FEI number is 3014241760.

What types of violations has YURANY ANDREA JIMENEZ MUNOZ received?

YURANY ANDREA JIMENEZ MUNOZ 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 YURANY ANDREA JIMENEZ MUNOZ come from?

All FDA import refusal data for YURANY ANDREA JIMENEZ MUNOZ 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.