Laurel Enterprise Corporation
⚠️ Moderate Risk
FEI: 1000231050 • Taipei Hsien, Chung Ho • TAIWAN
FEI Number
1000231050
Location
Taipei Hsien, Chung Ho
Country
TAIWANAddress
Sec. 2, 329 Chung Shan Rd, Section 2, Taipei Hsien, Chung Ho, Taiwan
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
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 |
|---|---|---|---|
| 12/16/2010 | 16PGD07CUTTLEFISH, CAKES, BALLS, ETC., OTHER AQUATIC SPECIES | 9SALMONELLA | New York District Office (NYK-DO) |
| 2/28/2006 | 16CGT99FISH CAKES, BALLS, ETC., N.E.C. | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 2/28/2006 | 16CGT99FISH CAKES, BALLS, ETC., N.E.C. | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
| 2/2/2004 | 16CGT99FISH CAKES, BALLS, ETC., N.E.C. | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
| 3/12/2003 | 16CGT99FISH CAKES, BALLS, ETC., N.E.C. | 9SALMONELLA | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Laurel Enterprise Corporation's FDA import refusal history?
Laurel Enterprise Corporation (FEI: 1000231050) has 5 FDA import refusal record(s) in our database, spanning from 3/12/2003 to 12/16/2010.
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. Laurel Enterprise Corporation's FEI number is 1000231050.
What types of violations has Laurel Enterprise Corporation received?
Laurel Enterprise Corporation 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 Laurel Enterprise Corporation come from?
All FDA import refusal data for Laurel Enterprise Corporation 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.