Frescomar Seaheim Corp
⚠️ High Risk
FEI: 3006535098 • South Cotabato, Socsargen • PHILIPPINES
FEI Number
3006535098
Location
South Cotabato, Socsargen
Country
PHILIPPINESAddress
No 5 2/F, Refrigeration Bldg., Fish, , South Cotabato, Socsargen, 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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/7/2009 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/7/2009 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/7/2009 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 4/7/2009 | 16AGT45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.) | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Frescomar Seaheim Corp's FDA import refusal history?
Frescomar Seaheim Corp (FEI: 3006535098) has 4 FDA import refusal record(s) in our database, spanning from 4/7/2009 to 4/7/2009.
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. Frescomar Seaheim Corp's FEI number is 3006535098.
What types of violations has Frescomar Seaheim Corp received?
Frescomar Seaheim Corp 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 Frescomar Seaheim Corp come from?
All FDA import refusal data for Frescomar Seaheim Corp 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.