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Kemon Spa

⚠️ Moderate Risk

FEI: 1000578826 • San Giustino, Perugia • ITALY

FEI

FEI Number

1000578826

📍

Location

San Giustino, Perugia

🇮🇹

Country

ITALY
🏢

Address

Via Enrico Mattei 35, Zona Industriale Altomare, San Giustino, Perugia, Italy

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
4/12/2012
Latest Refusal
4/12/2012
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

4713×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
4/12/2012
53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Los Angeles District Office (LOS-DO)
4/12/2012
53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Los Angeles District Office (LOS-DO)
4/12/2012
53EA02HAIR SPRAYS (AEROSOL FIXATIVES) (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kemon Spa's FDA import refusal history?

Kemon Spa (FEI: 1000578826) has 3 FDA import refusal record(s) in our database, spanning from 4/12/2012 to 4/12/2012.

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. Kemon Spa's FEI number is 1000578826.

What types of violations has Kemon Spa received?

Kemon Spa 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 Kemon Spa come from?

All FDA import refusal data for Kemon Spa 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.