El Jay Associates
⚠️ High Risk
FEI: 3003360795 • Georgetown • GUYANA
FEI Number
3003360795
Location
Georgetown
Country
GUYANAAddress
Land Of Canaan, Public Road 5, Georgetown, , Guyana
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
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 |
|---|---|---|---|
| 6/30/2006 | 16AGD99FISH, N.E.C. | 9SALMONELLA | New York District Office (NYK-DO) |
| 11/19/2004 | 16AGD47WEAKFISH (SEA TROUT) | 9SALMONELLA | Philadelphia District Office (PHI-DO) |
| 11/19/2004 | 16AGD47WEAKFISH (SEA TROUT) | 9SALMONELLA | Philadelphia District Office (PHI-DO) |
| 11/19/2004 | 16AGD08BUTTERFISH | 9SALMONELLA | Philadelphia District Office (PHI-DO) |
| 9/18/2002 | 16AGD08BUTTERFISH | 9SALMONELLA | Philadelphia District Office (PHI-DO) |
| 8/2/2002 | 16AGD47WEAKFISH (SEA TROUT) | 9SALMONELLA | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is El Jay Associates's FDA import refusal history?
El Jay Associates (FEI: 3003360795) has 6 FDA import refusal record(s) in our database, spanning from 8/2/2002 to 6/30/2006.
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. El Jay Associates's FEI number is 3003360795.
What types of violations has El Jay Associates received?
El Jay Associates 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 El Jay Associates come from?
All FDA import refusal data for El Jay Associates 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.