ImportRefusal LogoImportRefusal

Laproff

⚠️ High Risk

FEI: 3011084409 • Medellin • COLOMBIA

FEI

FEI Number

3011084409

📍

Location

Medellin

🇨🇴

Country

COLOMBIA
🏢

Address

Cra 453a 61 Sur, , Medellin, , Colombia

High Risk

FDA Import Risk Assessment

59.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
8/29/2025
Latest Refusal
11/12/2014
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
78.2×20%
Frequency
3.7×10%
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

754×

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
8/29/2025
64TDY08TACROLIMUS (IMMUNOSUPPRESSIVE)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/15/2023
56CCB27CEPHALEXIN (CEPHALOSPORINS)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/15/2023
62GCB99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/12/2014
61XDA45CETIRIZINE HYDROCHLORIDE (ANTI-HISTAMINIC)
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Laproff's FDA import refusal history?

Laproff (FEI: 3011084409) has 4 FDA import refusal record(s) in our database, spanning from 11/12/2014 to 8/29/2025.

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. Laproff's FEI number is 3011084409.

What types of violations has Laproff received?

Laproff 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 Laproff come from?

All FDA import refusal data for Laproff 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.