Mercedes Paez Guerrero
✅ Low Risk
FEI: 3009056090 • Bogoto • COLOMBIA
FEI Number
3009056090
Location
Bogoto
Country
COLOMBIAAddress
Cra 69d #24-15 Intu Apt 201, , Bogoto, , Colombia
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/23/2011 | 66VCE99MISCELLANEOUS PATENT MEDICINES, ETC. | 473LABELING | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Mercedes Paez Guerrero's FDA import refusal history?
Mercedes Paez Guerrero (FEI: 3009056090) has 1 FDA import refusal record(s) in our database, spanning from 8/23/2011 to 8/23/2011.
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. Mercedes Paez Guerrero's FEI number is 3009056090.
What types of violations has Mercedes Paez Guerrero received?
Mercedes Paez Guerrero 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 Mercedes Paez Guerrero come from?
All FDA import refusal data for Mercedes Paez Guerrero 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.