Maria Munoz
⚠️ Moderate Risk
FEI: 3003828574 • Santo Domingo De Guzman, Distrito Nacional • DOMINICAN REPUBLIC
FEI Number
3003828574
Location
Santo Domingo De Guzman, Distrito Nacional
Country
DOMINICAN REPUBLICAddress
Unknown Street, , Santo Domingo De Guzman, Distrito Nacional, Dominican Republic
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/3/2002 | 53EY01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | 198COLOR LBLG | San Juan District Office (SJN-DO) |
| 12/3/2002 | 53EY06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | 198COLOR LBLG | San Juan District Office (SJN-DO) |
| 12/3/2002 | 61HAL99ANTI-BACTERIAL, N.E.C. | 118NOT LISTED | San Juan District Office (SJN-DO) |
Frequently Asked Questions
What is Maria Munoz's FDA import refusal history?
Maria Munoz (FEI: 3003828574) has 3 FDA import refusal record(s) in our database, spanning from 12/3/2002 to 12/3/2002.
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. Maria Munoz's FEI number is 3003828574.
What types of violations has Maria Munoz received?
Maria Munoz 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 Maria Munoz come from?
All FDA import refusal data for Maria Munoz 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.