Pacific Northwest Herb Co
⚠️ Moderate Risk
FEI: 3002721517 • Coldstream, BC • CANADA
FEI Number
3002721517
Location
Coldstream, BC
Country
CANADAAddress
9792 Springfield Rd, , Coldstream, BC, Canada
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
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
Frequently Asked Questions
What is Pacific Northwest Herb Co's FDA import refusal history?
Pacific Northwest Herb Co (FEI: 3002721517) has 2 FDA import refusal record(s) in our database, spanning from 12/1/2011 to 12/27/2011.
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. Pacific Northwest Herb Co's FEI number is 3002721517.
What types of violations has Pacific Northwest Herb Co received?
Pacific Northwest Herb Co 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 Pacific Northwest Herb Co come from?
All FDA import refusal data for Pacific Northwest Herb Co 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.