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CHONGQING DERON INSTRUMENT MANUF

⚠️ Moderate Risk

FEI: 3013156161 • Chongqing • CHINA

FEI

FEI Number

3013156161

📍

Location

Chongqing

🇨🇳

Country

CHINA
🏢

Address

Rm 3-3-3, 50 Bldg, Yife, , Chongqing, , China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/20/2018
Latest Refusal
3/20/2018
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

4761×

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
3/20/2018
95REQRANGING (GEODIMETER) LASER PRODUCTS, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
476NO REGISTR
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is CHONGQING DERON INSTRUMENT MANUF's FDA import refusal history?

CHONGQING DERON INSTRUMENT MANUF (FEI: 3013156161) has 1 FDA import refusal record(s) in our database, spanning from 3/20/2018 to 3/20/2018.

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. CHONGQING DERON INSTRUMENT MANUF's FEI number is 3013156161.

What types of violations has CHONGQING DERON INSTRUMENT MANUF received?

CHONGQING DERON INSTRUMENT MANUF 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 CHONGQING DERON INSTRUMENT MANUF come from?

All FDA import refusal data for CHONGQING DERON INSTRUMENT MANUF 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.