Zesto Corporation
⚠️ Moderate Risk
FEI: 3005875933 • Metro Manila • PHILIPPINES
FEI Number
3005875933
Location
Metro Manila
Country
PHILIPPINESAddress
Novaliches, Quebec City, , Metro Manila, , Philippines
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
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
Frequently Asked Questions
What is Zesto Corporation's FDA import refusal history?
Zesto Corporation (FEI: 3005875933) has 2 FDA import refusal record(s) in our database, spanning from 11/8/2006 to 11/16/2006.
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. Zesto Corporation's FEI number is 3005875933.
What types of violations has Zesto Corporation received?
Zesto 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 Zesto Corporation come from?
All FDA import refusal data for Zesto 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.