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Ningbo Sunlight Electronics Co. Ltd

Low Risk

FEI: 3012081197 • Cixi City, ZHEJIANG • CHINA

FEI

FEI Number

3012081197

📍

Location

Cixi City, ZHEJIANG

🇨🇳

Country

CHINA
🏢

Address

NO.518, GUANSHEN ROAD NORTH, IDONG INDUSTRIAL ZONE, LONGSHAN TOWN, Cixi City, ZHEJIANG, China

Low Risk

FDA Import Risk Assessment

17.8
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
2/3/2022
Latest Refusal
2/3/2022
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
7.2×20%
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

2781×

NO TAG

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 to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

Refusal History

DateProductViolationsDivision
2/3/2022
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
278NO TAG
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Ningbo Sunlight Electronics Co. Ltd's FDA import refusal history?

Ningbo Sunlight Electronics Co. Ltd (FEI: 3012081197) has 1 FDA import refusal record(s) in our database, spanning from 2/3/2022 to 2/3/2022.

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. Ningbo Sunlight Electronics Co. Ltd's FEI number is 3012081197.

What types of violations has Ningbo Sunlight Electronics Co. Ltd received?

Ningbo Sunlight Electronics Co. Ltd 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 Ningbo Sunlight Electronics Co. Ltd come from?

All FDA import refusal data for Ningbo Sunlight Electronics Co. Ltd 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.