ADMICHONTA S.A.
⚠️ Moderate Risk
FEI: 3013190696 • Santo Domingo De Onzole • ECUADOR
FEI Number
3013190696
Location
Santo Domingo De Onzole
Country
ECUADORAddress
Km 8 Via Chone, , Santo Domingo De Onzole, , Ecuador
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
Frequently Asked Questions
What is ADMICHONTA S.A.'s FDA import refusal history?
ADMICHONTA S.A. (FEI: 3013190696) has 2 FDA import refusal record(s) in our database, spanning from 4/30/2018 to 5/13/2021.
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. ADMICHONTA S.A.'s FEI number is 3013190696.
What types of violations has ADMICHONTA S.A. received?
ADMICHONTA S.A. 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 ADMICHONTA S.A. come from?
All FDA import refusal data for ADMICHONTA S.A. 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.