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Chongqing Deron Instrument Manufacture Co, Ltd.

✅ Low Risk

FEI: 3009734103 • Chongqing • CHINA

FEI

FEI Number

3009734103

📍

Location

Chongqing

🇨🇳

Country

CHINA
🏢

Address

Rm 3-3-3, No 50 Bldg, Yifeng Garden, No, , Chongqing, , China

Low Risk

FDA Import Risk Assessment

16.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/5/2015
Latest Refusal
6/5/2015
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
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

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
6/5/2015
95RETLASER TARGET DESIGNATOR, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
278NO TAG
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Chongqing Deron Instrument Manufacture Co, Ltd.'s FDA import refusal history?

Chongqing Deron Instrument Manufacture Co, Ltd. (FEI: 3009734103) has 1 FDA import refusal record(s) in our database, spanning from 6/5/2015 to 6/5/2015.

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 Manufacture Co, Ltd.'s FEI number is 3009734103.

What types of violations has Chongqing Deron Instrument Manufacture Co, Ltd. received?

Chongqing Deron Instrument Manufacture 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 Chongqing Deron Instrument Manufacture Co, Ltd. come from?

All FDA import refusal data for Chongqing Deron Instrument Manufacture 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.