Hindustan Lever Ltd.
⚠️ Moderate Risk
FEI: 3003996709 • Bangalore, Karnataka • INDIA
FEI Number
3003996709
Location
Bangalore, Karnataka
Country
INDIAAddress
3rd Floor, 18 Ramanashree Arcase, Bangalore, Karnataka, 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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/3/2005 | 16XGT21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | Florida District Office (FLA-DO) | |
| 1/26/2005 | 16XGN21SHRIMP AND PRAWNS, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS | Florida District Office (FLA-DO) | |
| 3/8/2004 | 16JEE01CRAB | 249FILTHY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Hindustan Lever Ltd.'s FDA import refusal history?
Hindustan Lever Ltd. (FEI: 3003996709) has 3 FDA import refusal record(s) in our database, spanning from 3/8/2004 to 6/3/2005.
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. Hindustan Lever Ltd.'s FEI number is 3003996709.
What types of violations has Hindustan Lever Ltd. received?
Hindustan Lever 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 Hindustan Lever Ltd. come from?
All FDA import refusal data for Hindustan Lever 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.