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Rebecca Amoah

⚠️ Moderate Risk

FEI: 3004552790 • Accra • GHANA

FEI

FEI Number

3004552790

📍

Location

Accra

🇬🇭

Country

GHANA
🏢

Address

2021 Kotobaby Street 2nd Fl, , Accra, , Ghana

Moderate Risk

FDA Import Risk Assessment

33.1
LowModerateHighCritical

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

Statistics

9
Total Refusals
10
Unique Violations
5/28/2013
Latest Refusal
9/27/2006
Earliest Refusal

Score Breakdown

Violation Severity
51.5×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
13.5×10%
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

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.

3242×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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.

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

3211×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3301×

UNSAFE COL

The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).

4831×

DRUG NAME

The article appears to be a drug and fails to bear the proprietary or established name and/or name and quantity of each active ingredient.

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

91×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

2181×

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.

Refusal History

DateProductViolationsDivision
5/28/2013
25JFH16CASSAVA (ROOT AND TUBER VEGETABLE)
320LACKS FIRM
Division of Northeast Imports (DNEI)
6/29/2012
24AFH23OTHER BEAN/SEED SPROUTS, N.E.C.
324NO ENGLISH
Division of Northeast Imports (DNEI)
6/29/2012
02GFT99FLOURS AND MEALS N.E.C.
324NO ENGLISH
Division of Northeast Imports (DNEI)
5/31/2011
24AFH07KIDNEY BEAN
218LIST INGRE
320LACKS FIRM
New York District Office (NYK-DO)
5/16/2011
28EFT03FIVE SPICE MIX, WITHOUT SALT
253STD IDENT
320LACKS FIRM
321LACKS N/C
New York District Office (NYK-DO)
5/16/2011
28EFT03FIVE SPICE MIX, WITHOUT SALT
9SALMONELLA
New York District Office (NYK-DO)
5/4/2011
64ABJ20TRICLOSAN (DISINFECTANT)
330UNSAFE COL
483DRUG NAME
New York District Office (NYK-DO)
12/3/2009
16IFT21HERRING, HOT SMOKED, FISH
308MFR INSAN
New York District Office (NYK-DO)
9/27/2006
29BCT06SOFT DRINK, IMITATION FRUIT FLAVORED, CARBONATED
11UNSAFE COL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Rebecca Amoah's FDA import refusal history?

Rebecca Amoah (FEI: 3004552790) has 9 FDA import refusal record(s) in our database, spanning from 9/27/2006 to 5/28/2013.

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. Rebecca Amoah's FEI number is 3004552790.

What types of violations has Rebecca Amoah received?

Rebecca Amoah has been cited for 10 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 Rebecca Amoah come from?

All FDA import refusal data for Rebecca Amoah 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.