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Beijing Brighty Instrument Co

⚠️ Moderate Risk

FEI: 3006122917 • Beijing, Beijing • CHINA

FEI

FEI Number

3006122917

📍

Location

Beijing, Beijing

🇨🇳

Country

CHINA
🏢

Address

6 Weiyilu, Fengtai, Beijing, Beijing, China

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/18/2008
Latest Refusal
3/18/2008
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

21201×

UNSFDIETSP

The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.

Refusal History

DateProductViolationsDivision
3/18/2008
53PH99OTHER COSMETIC RAW MATERIALS, N.E.C.
2120UNSFDIETSP
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Beijing Brighty Instrument Co's FDA import refusal history?

Beijing Brighty Instrument Co (FEI: 3006122917) has 1 FDA import refusal record(s) in our database, spanning from 3/18/2008 to 3/18/2008.

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. Beijing Brighty Instrument Co's FEI number is 3006122917.

What types of violations has Beijing Brighty Instrument Co received?

Beijing Brighty Instrument Co 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 Beijing Brighty Instrument Co come from?

All FDA import refusal data for Beijing Brighty Instrument Co 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.