Del Centro, S.A. de C.V.
⚠️ Moderate Risk
FEI: 3004285132 • Irapuato, Guanajuato • MEXICO
FEI Number
3004285132
Location
Irapuato, Guanajuato
Country
MEXICOAddress
Av. Paseo Solidaridad No. 10323, , Irapuato, Guanajuato, 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
NEEDS ACID
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate acidification.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/26/2007 | 24FEI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 48NEEDS ACID | Southwest Import District Office (SWI-DO) |
| 6/26/2007 | 24FEI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 48NEEDS ACID | Southwest Import District Office (SWI-DO) |
| 6/26/2007 | 24FEI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 48NEEDS ACID | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Del Centro, S.A. de C.V.'s FDA import refusal history?
Del Centro, S.A. de C.V. (FEI: 3004285132) has 3 FDA import refusal record(s) in our database, spanning from 6/26/2007 to 6/26/2007.
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. Del Centro, S.A. de C.V.'s FEI number is 3004285132.
What types of violations has Del Centro, S.A. de C.V. received?
Del Centro, S.A. de C.V. 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 Del Centro, S.A. de C.V. come from?
All FDA import refusal data for Del Centro, S.A. de C.V. 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.