REGAL BELOIT DE GUADALAJARA
⚠️ High Risk
FEI: 3013473361 • El Salto • MEXICO
FEI Number
3013473361
Location
El Salto
Country
MEXICOAddress
Carr Guad KM 11.4, , El Salto, , Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/3/2025 | 95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL | 47NON STD | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is REGAL BELOIT DE GUADALAJARA's FDA import refusal history?
REGAL BELOIT DE GUADALAJARA (FEI: 3013473361) has 1 FDA import refusal record(s) in our database, spanning from 7/3/2025 to 7/3/2025.
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. REGAL BELOIT DE GUADALAJARA's FEI number is 3013473361.
What types of violations has REGAL BELOIT DE GUADALAJARA received?
REGAL BELOIT DE GUADALAJARA 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 REGAL BELOIT DE GUADALAJARA come from?
All FDA import refusal data for REGAL BELOIT DE GUADALAJARA 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.