Maria del Socorro Avila Rendon
⚠️ Moderate Risk
FEI: 3011287358 • Guadalajara, Jalisco • MEXICO
FEI Number
3011287358
Location
Guadalajara, Jalisco
Country
MEXICOAddress
Calle Cerro Del Borrego No 1114, Col. LOMAS INDEPENDENCIA, Guadalajara, 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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
INCONSPICU
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/7/2015 | 33AGT02CARAMEL CANDY PIECES, HARD, WITH NUTS OR NUT PRODUCTS (NOT COCONUT) (WITHOUT CHOCOLATE) | 297AFLATOXIN | Southwest Import District Office (SWI-DO) |
| 11/18/2013 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 11/18/2013 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 11/18/2013 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 11/7/2012 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 11/7/2012 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 11/7/2012 | 23BGT07PEANUT, SHELLED | Southwest Import District Office (SWI-DO) | |
| 9/14/2012 | 23BGT07PEANUT, SHELLED | 297AFLATOXIN | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Maria del Socorro Avila Rendon's FDA import refusal history?
Maria del Socorro Avila Rendon (FEI: 3011287358) has 8 FDA import refusal record(s) in our database, spanning from 9/14/2012 to 5/7/2015.
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. Maria del Socorro Avila Rendon's FEI number is 3011287358.
What types of violations has Maria del Socorro Avila Rendon received?
Maria del Socorro Avila Rendon has been cited for 4 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 Maria del Socorro Avila Rendon come from?
All FDA import refusal data for Maria del Socorro Avila Rendon 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.