DHARAMPAL PREMCHAND LTD
⚠️ High Risk
FEI: 3023201017 • Noida, Uttar Pradesh • INDIA
FEI Number
3023201017
Location
Noida, Uttar Pradesh
Country
INDIAAddress
Unit: A - 34, & 35, Noida, Uttar Pradesh, 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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
POISONORD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance which would ordinarily render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/10/2025 | 23BYT14BETEL NUT, SHELLED | 238UNSAFE ADD | Division of Southeast Imports (DSEI) |
| 9/25/2025 | 23FYY14BETEL NUT, TOPPING | 3878POISONORD | Division of Southeast Imports (DSEI) |
| 12/18/2023 | 23AGT14BETEL NUT, IN SHELL | Division of Southeast Imports (DSEI) | |
| 10/4/2023 | 23BET14BETEL NUT, SHELLED | 238UNSAFE ADD | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is DHARAMPAL PREMCHAND LTD's FDA import refusal history?
DHARAMPAL PREMCHAND LTD (FEI: 3023201017) has 4 FDA import refusal record(s) in our database, spanning from 10/4/2023 to 11/10/2025.
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. DHARAMPAL PREMCHAND LTD's FEI number is 3023201017.
What types of violations has DHARAMPAL PREMCHAND LTD received?
DHARAMPAL PREMCHAND LTD 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 DHARAMPAL PREMCHAND LTD come from?
All FDA import refusal data for DHARAMPAL PREMCHAND LTD 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.