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Dermocell Colombia Ltda

⚠️ Moderate Risk

FEI: 3004869282 • Bogota • COLOMBIA

FEI

FEI Number

3004869282

📍

Location

Bogota

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 108a No 1612, , Bogota, , Colombia

Moderate Risk

FDA Import Risk Assessment

35.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
7/27/2006
Latest Refusal
7/27/2006
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
7/27/2006
89IMIDIATHERMY, ULTRASONIC, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT
508NO 510(K)
Division of Southeast Imports (DSEI)
7/27/2006
89IPFSTIMULATOR, MUSCLE, POWERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Dermocell Colombia Ltda's FDA import refusal history?

Dermocell Colombia Ltda (FEI: 3004869282) has 2 FDA import refusal record(s) in our database, spanning from 7/27/2006 to 7/27/2006.

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. Dermocell Colombia Ltda's FEI number is 3004869282.

What types of violations has Dermocell Colombia Ltda received?

Dermocell Colombia Ltda 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 Dermocell Colombia Ltda come from?

All FDA import refusal data for Dermocell Colombia Ltda 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.