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Sonitronies S.A. De C.V. Dept. Arrow

⚠️ Moderate Risk

FEI: 3011775304 • Nogales, Sonora • MEXICO

FEI

FEI Number

3011775304

📍

Location

Nogales, Sonora

🇲🇽

Country

MEXICO
🏢

Address

Callejon Luis Donaldo Colosio 1179, Col. J. KALITEA, Nogales, Sonora, Mexico

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
6/6/2019
Latest Refusal
6/6/2019
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4763×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
6/6/2019
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of Southwest Imports (DSWI)
6/6/2019
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of Southwest Imports (DSWI)
6/6/2019
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
476NO REGISTR
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Sonitronies S.A. De C.V. Dept. Arrow's FDA import refusal history?

Sonitronies S.A. De C.V. Dept. Arrow (FEI: 3011775304) has 3 FDA import refusal record(s) in our database, spanning from 6/6/2019 to 6/6/2019.

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. Sonitronies S.A. De C.V. Dept. Arrow's FEI number is 3011775304.

What types of violations has Sonitronies S.A. De C.V. Dept. Arrow received?

Sonitronies S.A. De C.V. Dept. Arrow 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 Sonitronies S.A. De C.V. Dept. Arrow come from?

All FDA import refusal data for Sonitronies S.A. De C.V. Dept. Arrow 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.