HENACENT LIMITED
⚠️ High Risk
FEI: 3010267853 • Lashibi, GH-AA • GHANA
FEI Number
3010267853
Location
Lashibi, GH-AA
Country
GHANAAddress
125 B NUNGUA, , Lashibi, GH-AA, Ghana
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
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).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
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).
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.
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.
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.
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).
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.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/10/2024 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 7/10/2024 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 7/10/2024 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 7/10/2024 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 9/27/2019 | 26CHT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 9/27/2019 | 26CHT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 9/27/2019 | 26CHT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 9/27/2019 | 26CHT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 8/3/2018 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 5/23/2018 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 4/16/2018 | 28AGH99WHOLE SPICE, N.E.C. | Division of Northeast Imports (DNEI) | |
| 4/16/2018 | 23BGT07PEANUT, SHELLED | Division of Northeast Imports (DNEI) | |
| 4/13/2018 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 3/4/2014 | 63VDY02HYDROQUINONE (DEPIGMENTOR) | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 1/16/2014 | 56YDJ99ANTIBIOTIC N.E.C. | Division of Northeast Imports (DNEI) | |
| 9/5/2013 | 66VCY99MISCELLANEOUS PATENT MEDICINES, ETC. | 223FALSE | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is HENACENT LIMITED's FDA import refusal history?
HENACENT LIMITED (FEI: 3010267853) has 16 FDA import refusal record(s) in our database, spanning from 9/5/2013 to 7/10/2024.
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. HENACENT LIMITED's FEI number is 3010267853.
What types of violations has HENACENT LIMITED received?
HENACENT LIMITED 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 HENACENT LIMITED come from?
All FDA import refusal data for HENACENT 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.