A- ADUTWUMWAA ENTERPRISE
⚠️ Moderate Risk
FEI: 3011060409 • Accra, GH-AA • GHANA
FEI Number
3011060409
Location
Accra, GH-AA
Country
GHANAAddress
17 Kumbaya Street Achimota, , Accra, GH-AA, Ghana
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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.
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.
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.
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.
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.
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).
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).
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.
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/22/2017 | 63HBE99CATHARTIC N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 02HGT01TAPIOCA STARCH PRODUCT | 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 | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 29BCT99CARBONATED SOFT DRINK, N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/8/2017 | 62IAY99ANTI-NEOPLASTIC N.E.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.