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Laboratorios Coaspharma

⚠️ High Risk

FEI: 3008818240 • Bogota, Cundinamarca • COLOMBIA

FEI

FEI Number

3008818240

📍

Location

Bogota, Cundinamarca

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 18 # 28a-43, , Bogota, Cundinamarca, Colombia

High Risk

FDA Import Risk Assessment

64.2
LowModerateHighCritical

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

Statistics

13
Total Refusals
3
Unique Violations
10/22/2025
Latest Refusal
9/6/2019
Earliest Refusal

Score Breakdown

Violation Severity
82.5×40%
Refusal Volume
42.5×30%
Recency
81.5×20%
Frequency
21.2×10%
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

7513×

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).

1182×

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
10/22/2025
56YCJ99ANTIBIOTIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/22/2025
54AFJ16VITAMIN E (TOCOPHEROL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/27/2025
64LCA56PREDNISONE (GLUCOCORTICOID)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/10/2025
65RDR18SODIUM BICARBONATE (REPLENISHER)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/26/2025
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/13/2024
62GCC41IBUPROFEN (ANTI-INFLAMMATORY)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/13/2024
60WCY01ALBENDAZOLE (ANTHELMINTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/8/2021
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/28/2020
65PDY02SILDENAFIL CITRATE (REGULATOR)
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/24/2020
64XDY06SALICYLIC ACID (KERATOLYTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/25/2020
61WDY45FLUCONAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/2/2020
64LDJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/6/2019
60LDA01ACETAMINOPHEN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Laboratorios Coaspharma's FDA import refusal history?

Laboratorios Coaspharma (FEI: 3008818240) has 13 FDA import refusal record(s) in our database, spanning from 9/6/2019 to 10/22/2025.

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 Coaspharma's FEI number is 3008818240.

What types of violations has Laboratorios Coaspharma received?

Laboratorios Coaspharma has been cited for 3 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 Coaspharma come from?

All FDA import refusal data for Laboratorios Coaspharma 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.