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Inverpal

⚠️ Moderate Risk

FEI: 3007650343 • Barranquilla, Atlantico • COLOMBIA

FEI

FEI Number

3007650343

📍

Location

Barranquilla, Atlantico

🇨🇴

Country

COLOMBIA
🏢

Address

Carrera 47 No. 85-75, , Barranquilla, Atlantico, Colombia

Moderate Risk

FDA Import Risk Assessment

25.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/25/2010
Latest Refusal
10/25/2010
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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

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).

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
10/25/2010
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)
10/25/2010
73BXYFLOWMETER, CALIBRATION, GAS
118NOT LISTED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Inverpal's FDA import refusal history?

Inverpal (FEI: 3007650343) has 2 FDA import refusal record(s) in our database, spanning from 10/25/2010 to 10/25/2010.

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. Inverpal's FEI number is 3007650343.

What types of violations has Inverpal received?

Inverpal 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 Inverpal come from?

All FDA import refusal data for Inverpal 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.