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YUMNATURALS

⚠️ High Risk

FEI: 3016887624 • Minden, ON • CANADA

FEI

FEI Number

3016887624

📍

Location

Minden, ON

🇨🇦

Country

CANADA
🏢

Address

168 Bobcaygeon Road, , Minden, ON, Canada

High Risk

FDA Import Risk Assessment

63.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

4
Total Refusals
1
Unique Violations
8/11/2025
Latest Refusal
2/7/2025
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
77.0×20%
Frequency
40.0×10%
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

754×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
8/11/2025
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
8/11/2025
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/4/2025
66PBL99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/7/2025
65RDY19SODIUM CHLORIDE (REPLENISHER)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is YUMNATURALS's FDA import refusal history?

YUMNATURALS (FEI: 3016887624) has 4 FDA import refusal record(s) in our database, spanning from 2/7/2025 to 8/11/2025.

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. YUMNATURALS's FEI number is 3016887624.

What types of violations has YUMNATURALS received?

YUMNATURALS 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 YUMNATURALS come from?

All FDA import refusal data for YUMNATURALS 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.