Nouvelle Parfumerie Gandour Senegal
⚠️ Moderate Risk
FEI: 3008491314 • Dakar • SENEGAL
FEI Number
3008491314
Location
Dakar
Country
SENEGALAddress
Km 75 Route De Rufisque, , Dakar, , Senegal
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
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.
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).
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/12/2024 | 53LC06MOISTURIZING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 8/12/2024 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 10/5/2015 | 45LC99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | Seattle District Office (SEA-DO) | |
| 10/5/2015 | 45LC99FLAVORING AGENTS AND ADJUVANTS (FOOD ADDITIVES FOR HUMAN USE) | Seattle District Office (SEA-DO) | |
| 5/6/2015 | 26CCT01COCONUT OIL, REFINED, SINGLE INGREDIENT | Division of Northeast Imports (DNEI) | |
| 10/19/2010 | 63VDY02HYDROQUINONE (DEPIGMENTOR) | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Nouvelle Parfumerie Gandour Senegal's FDA import refusal history?
Nouvelle Parfumerie Gandour Senegal (FEI: 3008491314) has 6 FDA import refusal record(s) in our database, spanning from 10/19/2010 to 8/12/2024.
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. Nouvelle Parfumerie Gandour Senegal's FEI number is 3008491314.
What types of violations has Nouvelle Parfumerie Gandour Senegal received?
Nouvelle Parfumerie Gandour Senegal has been cited for 6 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 Nouvelle Parfumerie Gandour Senegal come from?
All FDA import refusal data for Nouvelle Parfumerie Gandour Senegal 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.