Tostadas Fanny S De Rl De Cv
⚠️ Moderate Risk
FEI: 3011097632 • Guanajuato • MEXICO
FEI Number
3011097632
Location
Guanajuato
Country
MEXICOAddress
Ave Pescadores No 120, , 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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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)).
USUAL NAME
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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/4/2016 | 03YGT09TORTILLAS | Division of Southwest Imports (DSWI) | |
| 7/7/2016 | 03YGT09TORTILLAS | Division of Southwest Imports (DSWI) | |
| 7/7/2016 | 03YGT09TORTILLAS | Division of Southwest Imports (DSWI) | |
| 7/7/2016 | 03BGT02BIALY PREPARED DRY MIX WITH MILK OR EGG | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Tostadas Fanny S De Rl De Cv's FDA import refusal history?
Tostadas Fanny S De Rl De Cv (FEI: 3011097632) has 4 FDA import refusal record(s) in our database, spanning from 7/7/2016 to 8/4/2016.
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. Tostadas Fanny S De Rl De Cv's FEI number is 3011097632.
What types of violations has Tostadas Fanny S De Rl De Cv received?
Tostadas Fanny S De Rl De Cv has been cited for 5 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 Tostadas Fanny S De Rl De Cv come from?
All FDA import refusal data for Tostadas Fanny S De Rl De Cv 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.