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DR OHIKHOBO

⚠️ Moderate Risk

FEI: 3012861982 • Ekpoma • NIGERIA

FEI

FEI Number

3012861982

📍

Location

Ekpoma

🇳🇬

Country

NIGERIA
🏢

Address

16 Iyamu Str Ekpoma, , Ekpoma, , Nigeria

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
11/8/2016
Latest Refusal
11/8/2016
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

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
11/8/2016
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
336INCONSPICU
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is DR OHIKHOBO's FDA import refusal history?

DR OHIKHOBO (FEI: 3012861982) has 1 FDA import refusal record(s) in our database, spanning from 11/8/2016 to 11/8/2016.

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. DR OHIKHOBO's FEI number is 3012861982.

What types of violations has DR OHIKHOBO received?

DR OHIKHOBO 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 DR OHIKHOBO come from?

All FDA import refusal data for DR OHIKHOBO 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.