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Dan Enterprise

⚠️ Moderate Risk

FEI: 3004765316 • Tema • GHANA

FEI

FEI Number

3004765316

📍

Location

Tema

🇬🇭

Country

GHANA
🏢

Address

P O Box 2868 Port Building, , Tema, , Ghana

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
5
Unique Violations
7/28/2005
Latest Refusal
7/28/2005
Earliest Refusal

Score Breakdown

Violation Severity
66.0×40%
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

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

30002×

N-RX INACT

The article appears to be a nonprescription drug and fails to bear the established name of each inactive ingredient in alphabetical order on the outside container of the retail package.

3442×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

752×

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
7/28/2005
63VBJ02HYDROQUINONE (DEPIGMENTOR)
16DIRECTIONS
3000N-RX INACT
344WARNINGS
473LABELING
75UNAPPROVED
Florida District Office (FLA-DO)
7/28/2005
64ABP20TRICLOSAN (DISINFECTANT)
16DIRECTIONS
3000N-RX INACT
344WARNINGS
473LABELING
75UNAPPROVED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Dan Enterprise's FDA import refusal history?

Dan Enterprise (FEI: 3004765316) has 2 FDA import refusal record(s) in our database, spanning from 7/28/2005 to 7/28/2005.

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. Dan Enterprise's FEI number is 3004765316.

What types of violations has Dan Enterprise received?

Dan Enterprise has been cited for 5 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 Dan Enterprise come from?

All FDA import refusal data for Dan Enterprise 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.