SESP GROUP
⚠️ High Risk
FEI: 3012787554 • Petakh Tikva • ISRAEL
FEI Number
3012787554
Location
Petakh Tikva
Country
ISRAELAddress
41, Ha-Sivim, , Petakh Tikva, , Israel
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
E COLI 157
The article appears to contain E. coli O157:H7 (EHEC), a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/3/2024 | 54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 3480E COLI 157 | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SESP GROUP's FDA import refusal history?
SESP GROUP (FEI: 3012787554) has 1 FDA import refusal record(s) in our database, spanning from 10/3/2024 to 10/3/2024.
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. SESP GROUP's FEI number is 3012787554.
What types of violations has SESP GROUP received?
SESP GROUP 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 SESP GROUP come from?
All FDA import refusal data for SESP GROUP 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.