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Vishay Precision Group Canada Ul

⚠️ Moderate Risk

FEI: 3010388369 • Toronto, Ontario • CANADA

FEI

FEI Number

3010388369

📍

Location

Toronto, Ontario

🇨🇦

Country

CANADA
🏢

Address

48 Lesmill Road, North York, Toronto, Ontario, Canada

Moderate Risk

FDA Import Risk Assessment

46.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
7/29/2024
Latest Refusal
7/29/2024
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
70.6×20%
Frequency
10.0×10%
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

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

Refusal History

DateProductViolationsDivision
7/29/2024
95REAHIGH-POWER LASER LIGHT SHOW PROJECTOR (OUTPUT>5MW)
47NON STD
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Vishay Precision Group Canada Ul's FDA import refusal history?

Vishay Precision Group Canada Ul (FEI: 3010388369) has 1 FDA import refusal record(s) in our database, spanning from 7/29/2024 to 7/29/2024.

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. Vishay Precision Group Canada Ul's FEI number is 3010388369.

What types of violations has Vishay Precision Group Canada Ul received?

Vishay Precision Group Canada Ul 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 Vishay Precision Group Canada Ul come from?

All FDA import refusal data for Vishay Precision Group Canada Ul 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.