ROSARIO ELIZABETH MONTERROSAS RO
⚠️ Moderate Risk
FEI: 3014678567 • Puebla, PUE • MEXICO
FEI Number
3014678567
Location
Puebla, PUE
Country
MEXICOAddress
11 Sur 306 Barrio San J, , Puebla, PUE, Mexico
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
Frequently Asked Questions
What is ROSARIO ELIZABETH MONTERROSAS RO's FDA import refusal history?
ROSARIO ELIZABETH MONTERROSAS RO (FEI: 3014678567) has 2 FDA import refusal record(s) in our database, spanning from 9/21/2018 to 9/21/2018.
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. ROSARIO ELIZABETH MONTERROSAS RO's FEI number is 3014678567.
What types of violations has ROSARIO ELIZABETH MONTERROSAS RO received?
ROSARIO ELIZABETH MONTERROSAS RO 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 ROSARIO ELIZABETH MONTERROSAS RO come from?
All FDA import refusal data for ROSARIO ELIZABETH MONTERROSAS RO 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.