DIAKITE OUSMANE
⚠️ Moderate Risk
FEI: 3015909594 • Abidjan • IVORY COAST
FEI Number
3015909594
Location
Abidjan
Country
IVORY COASTAddress
B281 Anyama, 225 Cote D Ivoire, Abidjan, , Ivory Coast
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
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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).
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
INSANITARY
The article is subject to refusal of admission pursuant to section 801(a)(3) in that the article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or whereby it may have been rendered injurious to health.
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 |
|---|---|---|---|
| 10/31/2019 | 33YGT99CANDY WITHOUT CHOCOLATE N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28FGY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28FGY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28BGY54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28BFY31ONION, GROUND, CRACKED (SPICE) | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28FGY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 37KGY99PASTES, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 02YHY99MILLED GRAIN PRODUCTS, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 36CHT04HONEY | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 28FGY99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 23DHY07PEANUT, PASTE | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 54FYT99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Southeast Imports (DSEI) | |
| 10/31/2019 | 21VHT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is DIAKITE OUSMANE's FDA import refusal history?
DIAKITE OUSMANE (FEI: 3015909594) has 15 FDA import refusal record(s) in our database, spanning from 10/31/2019 to 10/31/2019.
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. DIAKITE OUSMANE's FEI number is 3015909594.
What types of violations has DIAKITE OUSMANE received?
DIAKITE OUSMANE has been cited for 8 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 DIAKITE OUSMANE come from?
All FDA import refusal data for DIAKITE OUSMANE 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.