ImportRefusal LogoImportRefusal

Olabisi Akanji

⚠️ Moderate Risk

FEI: 3010043091 • Nigeria • NIGERIA

FEI

FEI Number

3010043091

📍

Location

Nigeria

🇳🇬

Country

NIGERIA
🏢

Address

Nigeria, , Nigeria, , Nigeria

Moderate Risk

FDA Import Risk Assessment

35.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
10/18/2013
Latest Refusal
10/18/2013
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

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).

751×

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).

Refusal History

DateProductViolationsDivision
10/18/2013
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
Atlanta District Office (ATL-DO)
10/18/2013
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
118NOT LISTED
Atlanta District Office (ATL-DO)
10/18/2013
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
75UNAPPROVED
Atlanta District Office (ATL-DO)

Frequently Asked Questions

What is Olabisi Akanji's FDA import refusal history?

Olabisi Akanji (FEI: 3010043091) has 3 FDA import refusal record(s) in our database, spanning from 10/18/2013 to 10/18/2013.

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. Olabisi Akanji's FEI number is 3010043091.

What types of violations has Olabisi Akanji received?

Olabisi Akanji 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 Olabisi Akanji come from?

All FDA import refusal data for Olabisi Akanji 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.