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CDR Productos, S.R.L.

⚠️ Moderate Risk

FEI: 3009427147 • Distrito Nacional, DO-01 • DOMINICAN REPUBLIC

FEI

FEI Number

3009427147

📍

Location

Distrito Nacional, DO-01

🇩🇴
🏢

Address

Ave. 27 De Febrero Esq. W. Churchill, Plaza Central, Distrito Nacional, DO-01, Dominican Republic

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
9/3/2013
Latest Refusal
9/3/2013
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

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
9/3/2013
53ED99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C.
473LABELING
San Juan District Office (SJN-DO)
9/3/2013
53ED99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C.
473LABELING
San Juan District Office (SJN-DO)
9/3/2013
53ED99OTHER HAIR PREPARATIONS, NON-COLORING), N.E.C.
473LABELING
San Juan District Office (SJN-DO)

Frequently Asked Questions

What is CDR Productos, S.R.L.'s FDA import refusal history?

CDR Productos, S.R.L. (FEI: 3009427147) has 3 FDA import refusal record(s) in our database, spanning from 9/3/2013 to 9/3/2013.

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. CDR Productos, S.R.L.'s FEI number is 3009427147.

What types of violations has CDR Productos, S.R.L. received?

CDR Productos, S.R.L. 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 CDR Productos, S.R.L. come from?

All FDA import refusal data for CDR Productos, S.R.L. 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.