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Claripack

⚠️ High Risk

FEI: 3005666197 • Bogota • COLOMBIA

FEI

FEI Number

3005666197

📍

Location

Bogota

🇨🇴

Country

COLOMBIA
🏢

Address

Cra 68c, No.11-75, , Bogota, , Colombia

High Risk

FDA Import Risk Assessment

58.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
11/4/2025
Latest Refusal
6/19/2019
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
95.9×20%
Frequency
4.7×10%
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

753×

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).

1181×

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).

Refusal History

DateProductViolationsDivision
11/4/2025
62GDY41IBUPROFEN (ANTI-INFLAMMATORY)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/28/2020
61HCY99ANTI-BACTERIAL, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/19/2019
62HCA03TROVAFLOXACIN/AZITHROMYCIN (ANTI-MICROBIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Claripack's FDA import refusal history?

Claripack (FEI: 3005666197) has 3 FDA import refusal record(s) in our database, spanning from 6/19/2019 to 11/4/2025.

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. Claripack's FEI number is 3005666197.

What types of violations has Claripack received?

Claripack 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 Claripack come from?

All FDA import refusal data for Claripack 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.