KISHORE EXPORT HOUSE
✅ Low Risk
FEI: 3014539962 • Gandhidham Sub-Distri • INDIA
FEI Number
3014539962
Location
Gandhidham Sub-Distri
Country
INDIAAddress
Shed No 407, N-Ii, Phase 2, Kandla Special Economic Zone, Gandhidham Sub-Distri, , India
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
TPNOWRNLBL
This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is a tobacco product which appears to be misbranded under section 903(a)(8)(B)(i) and 903(a)(1) because its package label does not include a brief statement of the relevant warnings (i.e., one of the four warnings required by section 3 of the Comprehensive Smokeless Tobacco Health Education Act).
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.
Refusal History
Frequently Asked Questions
What is KISHORE EXPORT HOUSE's FDA import refusal history?
KISHORE EXPORT HOUSE (FEI: 3014539962) has 1 FDA import refusal record(s) in our database, spanning from 5/11/2020 to 5/11/2020.
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. KISHORE EXPORT HOUSE's FEI number is 3014539962.
What types of violations has KISHORE EXPORT HOUSE received?
KISHORE EXPORT HOUSE has been cited for 2 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 KISHORE EXPORT HOUSE come from?
All FDA import refusal data for KISHORE EXPORT HOUSE 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.