Wilper Marketing
✅ Low Risk
FEI: 3003881311 • Caloocan City • PHILIPPINES
FEI Number
3003881311
Location
Caloocan City
Country
PHILIPPINESAddress
125-E D. Aquino St., , Caloocan City, , Philippines
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
Frequently Asked Questions
What is Wilper Marketing's FDA import refusal history?
Wilper Marketing (FEI: 3003881311) has 1 FDA import refusal record(s) in our database, spanning from 4/6/2004 to 4/6/2004.
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. Wilper Marketing's FEI number is 3003881311.
What types of violations has Wilper Marketing received?
Wilper Marketing has been cited for 2 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 Wilper Marketing come from?
All FDA import refusal data for Wilper Marketing 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.