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Clairol, Inc.

⚠️ Moderate Risk

FEI: 1211013 • Stamford, CT • UNITED STATES

FEI

FEI Number

1211013

📍

Location

Stamford, CT

🇺🇸
🏢

Address

1 Blachley Rd, , Stamford, CT, United States

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/27/2003
Latest Refusal
10/27/2003
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

1973×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

Refusal History

DateProductViolationsDivision
10/27/2003
53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
New York District Office (NYK-DO)
10/27/2003
53EC06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
New York District Office (NYK-DO)
10/27/2003
53EC06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
197COSM COLOR
New York District Office (NYK-DO)

Frequently Asked Questions

What is Clairol, Inc.'s FDA import refusal history?

Clairol, Inc. (FEI: 1211013) has 3 FDA import refusal record(s) in our database, spanning from 10/27/2003 to 10/27/2003.

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. Clairol, Inc.'s FEI number is 1211013.

What types of violations has Clairol, Inc. received?

Clairol, 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 Clairol, Inc. come from?

All FDA import refusal data for Clairol, 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.