PUJA GREH
⚠️ High Risk
FEI: 3014628400 • Delhi, Delhi • INDIA
FEI Number
3014628400
Location
Delhi, Delhi
Country
INDIAAddress
Street No, 1 Gali No 21, Delhi, Delhi, 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
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 |
|---|---|---|---|
| 12/26/2024 | 23BGT14BETEL NUT, SHELLED | 3878POISONORD | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is PUJA GREH's FDA import refusal history?
PUJA GREH (FEI: 3014628400) has 1 FDA import refusal record(s) in our database, spanning from 12/26/2024 to 12/26/2024.
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. PUJA GREH's FEI number is 3014628400.
What types of violations has PUJA GREH received?
PUJA GREH has been cited for 1 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 PUJA GREH come from?
All FDA import refusal data for PUJA GREH 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.