GOURI NDIA
⚠️ Moderate Risk
FEI: 3014313433 • Chandigarh • INDIA
FEI Number
3014313433
Location
Chandigarh
Country
INDIAAddress
136-140/67 Industrial Area Road, Industrial Area Phase 2, Chandigarh, , 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/5/2019 | 28KGH99SPICES AND SEASONING, GROUND, CRACKED, WITH SALT, N.E.C. | 249FILTHY | Division of Northern Border Imports (DNBI) |
| 2/5/2019 | 28AGH54PEPPER,BLACK, WHOLE (SPICE) | 249FILTHY | Division of Northern Border Imports (DNBI) |
| 2/5/2019 | 28BGH54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 157FOREIGN OB | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is GOURI NDIA's FDA import refusal history?
GOURI NDIA (FEI: 3014313433) has 3 FDA import refusal record(s) in our database, spanning from 2/5/2019 to 2/5/2019.
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. GOURI NDIA's FEI number is 3014313433.
What types of violations has GOURI NDIA received?
GOURI NDIA 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 GOURI NDIA come from?
All FDA import refusal data for GOURI NDIA 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.