CHIABLANCA, S.C. DE R.L.
⚠️ Moderate Risk
FEI: 3004861045 • Pueblo Acatic Centro, Jalisco • MEXICO
FEI Number
3004861045
Location
Pueblo Acatic Centro, Jalisco
Country
MEXICOAddress
Calle La Paz 54, Acatic, Pueblo Acatic Centro, Jalisco, 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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
Frequently Asked Questions
What is CHIABLANCA, S.C. DE R.L.'s FDA import refusal history?
CHIABLANCA, S.C. DE R.L. (FEI: 3004861045) has 2 FDA import refusal record(s) in our database, spanning from 6/22/2012 to 7/31/2012.
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. CHIABLANCA, S.C. DE R.L.'s FEI number is 3004861045.
What types of violations has CHIABLANCA, S.C. DE R.L. received?
CHIABLANCA, S.C. DE 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 CHIABLANCA, S.C. DE R.L. come from?
All FDA import refusal data for CHIABLANCA, S.C. DE 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.