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Chutima Saenyakul

✅ Low Risk

FEI: 3008303136 • Khao Kho • THAILAND

FEI

FEI Number

3008303136

📍

Location

Khao Kho

🇹🇭

Country

THAILAND
🏢

Address

10, Kham Noikhaokoh, Khao Kho, , Thailand

Low Risk

FDA Import Risk Assessment

24.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
5/5/2010
Latest Refusal
5/5/2010
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

4712×

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.

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
5/5/2010
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
471CSTIC LBLG
Cincinnati District Office (CIN-DO)
5/5/2010
53JY01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS)
118NOT LISTED
471CSTIC LBLG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Chutima Saenyakul's FDA import refusal history?

Chutima Saenyakul (FEI: 3008303136) has 2 FDA import refusal record(s) in our database, spanning from 5/5/2010 to 5/5/2010.

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. Chutima Saenyakul's FEI number is 3008303136.

What types of violations has Chutima Saenyakul received?

Chutima Saenyakul has been cited for 2 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 Chutima Saenyakul come from?

All FDA import refusal data for Chutima Saenyakul 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.