Supreme Worldwide
⚠️ High Risk
FEI: 3010580897 • -Thane • INDIA
FEI Number
3010580897
Location
-Thane
Country
INDIAAddress
Assangaon, , Shapur, Dust,-Thane, , India
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
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
COSMETFPLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.
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).
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
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.
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).
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/20/2024 | 50NGY18HENNA | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 9/20/2024 | 50NGY18HENNA | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 9/20/2024 | 50NGY18HENNA | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 9/20/2024 | 50NGY18HENNA | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/11/2024 | 50NGY18HENNA | Division of Northeast Imports (DNEI) | |
| 9/3/2024 | 50NHY18HENNA | 11UNSAFE COL | Division of Northeast Imports (DNEI) |
| 1/16/2024 | 53YH99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 3/7/2018 | 53YD99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | Division of Southwest Imports (DSWI) | |
| 1/4/2017 | 53YG99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | 197COSM COLOR | Division of Northeast Imports (DNEI) |
| 1/29/2015 | 53YG99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | 197COSM COLOR | New York District Office (NYK-DO) |
| 3/4/2014 | 53FH01HAIR DYES AND COLORS (ALL TYPES REQUIRE CAUTION STATEMENTS AND PATCH TESTS) (HAIR COLORING PREPARATI | 475COSMETLBLG | New York District Office (NYK-DO) |
| 3/4/2014 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Supreme Worldwide's FDA import refusal history?
Supreme Worldwide (FEI: 3010580897) has 20 FDA import refusal record(s) in our database, spanning from 3/4/2014 to 9/20/2024.
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. Supreme Worldwide's FEI number is 3010580897.
What types of violations has Supreme Worldwide received?
Supreme Worldwide 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 Supreme Worldwide come from?
All FDA import refusal data for Supreme Worldwide 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.