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NOVAMED LABS

⚠️ High Risk

FEI: 3013024177 • Bogota, Cundinamarca • COLOMBIA

FEI

FEI Number

3013024177

📍

Location

Bogota, Cundinamarca

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 72 12 65, , Bogota, Cundinamarca, Colombia

High Risk

FDA Import Risk Assessment

61.1
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
1/13/2026
Latest Refusal
3/20/2017
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
37.0×30%
Recency
91.3×20%
Frequency
10.2×10%
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

758×

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).

32802×

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
1/13/2026
61NCA83ESCITALOPRAM OXALATE
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/24/2025
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/29/2023
62TCE06ESOMEPRAZOLE MAGNESIUM (ANTI-SECRETORY)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/1/2022
62ODY41LOSARTAN POTASSIUM (ANTI-HYPERTENSIVE - PART II)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/17/2020
65RDY19SODIUM CHLORIDE (REPLENISHER)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/4/2020
61NDA29FLUOXETINE (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/12/2019
62GDY99ANTI-INFLAMMATORY N.E.C.
3280FRNMFGREG
Division of Southeast Imports (DSEI)
3/8/2019
62VCY01AMANTADINE HCL (ANTI-VIRAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/20/2017
66VCY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is NOVAMED LABS's FDA import refusal history?

NOVAMED LABS (FEI: 3013024177) has 9 FDA import refusal record(s) in our database, spanning from 3/20/2017 to 1/13/2026.

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. NOVAMED LABS's FEI number is 3013024177.

What types of violations has NOVAMED LABS received?

NOVAMED LABS 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 NOVAMED LABS come from?

All FDA import refusal data for NOVAMED LABS 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.