B. Terfloth
⚠️ Moderate Risk
FEI: 3003912046 • Westmount, Quebec • CANADA
FEI Number
3003912046
Location
Westmount, Quebec
Country
CANADAAddress
1 Westmount Car, , Westmount, Quebec, 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
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/21/2003 | 16AEE32SALMON (HUMPBACK, SILVER, KING, SOCKEYE, ETC.) | 62NEEDS FCE | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is B. Terfloth's FDA import refusal history?
B. Terfloth (FEI: 3003912046) has 1 FDA import refusal record(s) in our database, spanning from 4/21/2003 to 4/21/2003.
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. B. Terfloth's FEI number is 3003912046.
What types of violations has B. Terfloth received?
B. Terfloth 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 B. Terfloth come from?
All FDA import refusal data for B. Terfloth 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.