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Ana Celia Rodrig

✅ Low Risk

FEI: 3005710014 • Santiago • DOMINICAN REPUBLIC

FEI

FEI Number

3005710014

📍

Location

Santiago

🇩🇴
🏢

Address

Hatto Del Parque, , Santiago, , Dominican Republic

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
5/17/2006
Latest Refusal
5/17/2006
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
5/17/2006
53BD01BATH OILS, TABLETS AND SALTS (BATH PREPARATIONS)
471CSTIC LBLG
475COSMETLBLG
New Orleans District Office (NOL-DO)
5/17/2006
53BD01BATH OILS, TABLETS AND SALTS (BATH PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ana Celia Rodrig's FDA import refusal history?

Ana Celia Rodrig (FEI: 3005710014) has 2 FDA import refusal record(s) in our database, spanning from 5/17/2006 to 5/17/2006.

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. Ana Celia Rodrig's FEI number is 3005710014.

What types of violations has Ana Celia Rodrig received?

Ana Celia Rodrig 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 Ana Celia Rodrig come from?

All FDA import refusal data for Ana Celia Rodrig 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.