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BOATEMAA AND SONS COMPANY LIMITED

✅ Low Risk

FEI: 3027403612 • Accra, Greater Accra • GHANA

FEI

FEI Number

3027403612

📍

Location

Accra, Greater Accra

🇬🇭

Country

GHANA
🏢

Address

Ghana Assorted Foodstuff Exporter Association, 7 Behind Best Point Saving And Loan Bank, Achimota Mile, Accra, Greater Accra, Ghana

Low Risk

FDA Import Risk Assessment

24.7
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

3
Total Refusals
5
Unique Violations
10/27/2017
Latest Refusal
9/29/2017
Earliest Refusal

Score Breakdown

Violation Severity
37.5×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3202×

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.

3212×

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.

3282×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

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).

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
10/27/2017
28AGH99WHOLE SPICE, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
10/27/2017
28AGH99WHOLE SPICE, N.E.C.
320LACKS FIRM
321LACKS N/C
328USUAL NAME
Division of Northeast Imports (DNEI)
9/29/2017
62MOA99ANTI-PRURITIC N.E.C.
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is BOATEMAA AND SONS COMPANY LIMITED's FDA import refusal history?

BOATEMAA AND SONS COMPANY LIMITED (FEI: 3027403612) has 3 FDA import refusal record(s) in our database, spanning from 9/29/2017 to 10/27/2017.

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. BOATEMAA AND SONS COMPANY LIMITED's FEI number is 3027403612.

What types of violations has BOATEMAA AND SONS COMPANY LIMITED received?

BOATEMAA AND SONS COMPANY LIMITED 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 BOATEMAA AND SONS COMPANY LIMITED come from?

All FDA import refusal data for BOATEMAA AND SONS COMPANY LIMITED 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.