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Kaizen Inc

⚠️ Moderate Risk

FEI: 3003507417 • Gardena, CA • UNITED STATES

FEI

FEI Number

3003507417

📍

Location

Gardena, CA

🇺🇸
🏢

Address

13800 Gramercy Pl, , Gardena, CA, United States

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
7/25/2011
Latest Refusal
7/25/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

31201×

EPHEDALK

The product is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a dietary supplement or a dietary ingredient that appears to contain ephedrine alkaloids, which presents an unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling, or if no conditions of use are suggested in the labeling, under ordinary conditions of use.

Refusal History

DateProductViolationsDivision
7/25/2011
54FBB09EPHEDRA (HERBAL & BOTANICALS, NOT TEAS)
3120EPHEDALK
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Kaizen Inc's FDA import refusal history?

Kaizen Inc (FEI: 3003507417) has 1 FDA import refusal record(s) in our database, spanning from 7/25/2011 to 7/25/2011.

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. Kaizen Inc's FEI number is 3003507417.

What types of violations has Kaizen Inc received?

Kaizen Inc 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 Kaizen Inc come from?

All FDA import refusal data for Kaizen Inc 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.