EMARS ENTERPRISES
⚠️ High Risk
FEI: 1000283929 • Pangasinan, Ilicos Region • PHILIPPINES
FEI Number
1000283929
Location
Pangasinan, Ilicos Region
Country
PHILIPPINESAddress
59 Maniboc West, , Pangasinan, Ilicos Region, Philippines
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
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.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/4/2025 | 16YGT09FISH SAUCE, FISHERY PRODUCTS, N.E.C. | 249FILTHY | Division of West Coast Imports (DWCI) |
| 11/8/2011 | 16YEY09FISH SAUCE, FISHERY PRODUCTS, N.E.C. | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 9/19/2002 | 16YEP03FISH PASTE, FISHERY PRODUCTS, N.E.C. | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is EMARS ENTERPRISES's FDA import refusal history?
EMARS ENTERPRISES (FEI: 1000283929) has 3 FDA import refusal record(s) in our database, spanning from 9/19/2002 to 8/4/2025.
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. EMARS ENTERPRISES's FEI number is 1000283929.
What types of violations has EMARS ENTERPRISES received?
EMARS ENTERPRISES 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 EMARS ENTERPRISES come from?
All FDA import refusal data for EMARS ENTERPRISES 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.