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A- ADUTWUMWAA ENTERPRISE

⚠️ Moderate Risk

FEI: 3011060409 • Accra, GH-AA • GHANA

FEI

FEI Number

3011060409

📍

Location

Accra, GH-AA

🇬🇭

Country

GHANA
🏢

Address

17 Kumbaya Street Achimota, , Accra, GH-AA, Ghana

Moderate Risk

FDA Import Risk Assessment

45.0
LowModerateHighCritical

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

Statistics

17
Total Refusals
11
Unique Violations
9/22/2017
Latest Refusal
9/7/2017
Earliest Refusal

Score Breakdown

Violation Severity
52.7×40%
Refusal Volume
46.5×30%
Recency
0.0×20%
Frequency
100.0×10%
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

169×

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.

4824×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

2183×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3203×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

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.

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).

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).

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

2531×

STD IDENT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
9/22/2017
63HBE99CATHARTIC N.E.C.
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
75UNAPPROVED
Division of Northeast Imports (DNEI)
9/8/2017
02HGT01TAPIOCA STARCH PRODUCT
320LACKS FIRM
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/8/2017
28BGY60PEPPER, MIXED, GROUND, CRACKED (SPICE)
320LACKS FIRM
Division of Northeast Imports (DNEI)
9/8/2017
29BCT50SOFT DRINK, COLA, CARBONATED
253STD IDENT
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/8/2017
29BCT99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/8/2017
29BCT99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
482NUTRIT LBL
Division of Northeast Imports (DNEI)
9/8/2017
29BCT99CARBONATED SOFT DRINK, N.E.C.
218LIST INGRE
320LACKS FIRM
Division of Northeast Imports (DNEI)
9/8/2017
62IAY99ANTI-NEOPLASTIC N.E.C.
16DIRECTIONS
335LACKS N/C
Division of Northeast Imports (DNEI)
9/8/2017
64LDJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
63VBY02HYDROQUINONE (DEPIGMENTOR)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
63VBY02HYDROQUINONE (DEPIGMENTOR)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
61XDL14CYPROHEPTADINE HCL (ANTI-HISTAMINIC)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
64LDJ06BETAMETHASONE DIPROPIONATE (GLUCOCORTICOID)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
64LDJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
64LDJ67CLOBETASOL PROPIONATE (GLUCOCORTICOID)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/8/2017
64LDJ06BETAMETHASONE DIPROPIONATE (GLUCOCORTICOID)
16DIRECTIONS
Division of Northeast Imports (DNEI)
9/7/2017
63HBL99CATHARTIC N.E.C.
223FALSE
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is A- ADUTWUMWAA ENTERPRISE's FDA import refusal history?

A- ADUTWUMWAA ENTERPRISE (FEI: 3011060409) has 17 FDA import refusal record(s) in our database, spanning from 9/7/2017 to 9/22/2017.

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. A- ADUTWUMWAA ENTERPRISE's FEI number is 3011060409.

What types of violations has A- ADUTWUMWAA ENTERPRISE received?

A- ADUTWUMWAA ENTERPRISE has been cited for 11 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 A- ADUTWUMWAA ENTERPRISE come from?

All FDA import refusal data for A- ADUTWUMWAA 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.