Geo Medicore Limited
⚠️ High Risk
FEI: 3014869929 • Accra-Ghana • GHANA
FEI Number
3014869929
Location
Accra-Ghana
Country
GHANAAddress
Factory: Plot No. 312 to 315, Kuntunse, Accra-Ghana, , 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
ADDDRUGBIO
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a food to which has been added either a drug approved under section 505, a biological product licensed under section 351 of the Public Health Service Act, or a drug or a biological product for which substantial clinical investigations have been instituted and for which the existence of such investigations has been made public; and it appears that none of the exceptions listed in 301(ll)(1)-(4) applies.
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.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
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).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/12/2025 | 66VBY99MISCELLANEOUS PATENT MEDICINES, ETC. | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 1/6/2022 | 61XBY14CYPROHEPTADINE HCL (ANTI-HISTAMINIC) | 3887ADDDRUGBIO | Division of Northeast Imports (DNEI) |
| 7/2/2020 | 54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 3887ADDDRUGBIO | Division of Northeast Imports (DNEI) |
| 11/1/2018 | 61HAB11SULFATHIAZOLE | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Geo Medicore Limited's FDA import refusal history?
Geo Medicore Limited (FEI: 3014869929) has 4 FDA import refusal record(s) in our database, spanning from 11/1/2018 to 8/12/2025.
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. Geo Medicore Limited's FEI number is 3014869929.
What types of violations has Geo Medicore Limited received?
Geo Medicore Limited has been cited for 7 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 Geo Medicore Limited come from?
All FDA import refusal data for Geo Medicore 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.