KING INTERNATIONAL
⚠️ Moderate Risk
FEI: 3025603330 • New Delhi, Delhi • INDIA
FEI Number
3025603330
Location
New Delhi, Delhi
Country
INDIAAddress
4611-19, C- First Floor, Flat No. 203, Ansari Road, , New Delhi, Delhi, India
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
TP FLAVOR
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.
TPLACKFIRM
This article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(A) of the FD&C Act in that the label does not contain the name and place of business of the tobacco product manufacturer, packer or distributor.
TPLKUSSLLB
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.
TPLACKSNC
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(B) of the FD&C Act in that the label does not provide an accurate statement of the quantity of contents in terms of weight, measure or numerical count.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/16/2024 | 98FCA99ROLL-YOUR-OWN TOBACCO COMPONENT, PART OR ACCESSORY, NEC | Division of Southwest Imports (DSWI) | |
| 10/16/2024 | 98FCA99ROLL-YOUR-OWN TOBACCO COMPONENT, PART OR ACCESSORY, NEC | Division of Southwest Imports (DSWI) | |
| 10/16/2024 | 98FCA99ROLL-YOUR-OWN TOBACCO COMPONENT, PART OR ACCESSORY, NEC | Division of Southwest Imports (DSWI) | |
| 10/16/2024 | 98FCA99ROLL-YOUR-OWN TOBACCO COMPONENT, PART OR ACCESSORY, NEC | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is KING INTERNATIONAL's FDA import refusal history?
KING INTERNATIONAL (FEI: 3025603330) has 4 FDA import refusal record(s) in our database, spanning from 10/16/2024 to 10/16/2024.
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. KING INTERNATIONAL's FEI number is 3025603330.
What types of violations has KING INTERNATIONAL received?
KING INTERNATIONAL has been cited for 4 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 KING INTERNATIONAL come from?
All FDA import refusal data for KING INTERNATIONAL 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.