Procesos La Querendona S.A. de C.V.
⚠️ Moderate Risk
FEI: 3012304879 • Saltillo, Coahuila de Zaragoza • MEXICO
FEI Number
3012304879
Location
Saltillo, Coahuila de Zaragoza
Country
MEXICOAddress
Calle Julio Cervantes 612, Col. Heroes De Chapultepec, Saltillo, Coahuila de Zaragoza, 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.
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)).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/19/2024 | 27YCT06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Southwest Imports (DSWI) | |
| 11/19/2024 | 27YHT06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Southwest Imports (DSWI) | |
| 8/1/2022 | 27YHT06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Southwest Imports (DSWI) | |
| 8/1/2022 | 27YGT06PEPPER SAUCE (HOT, MILD, ETC.) | Division of Southwest Imports (DSWI) | |
| 4/22/2022 | 27YGI09SALSA | Division of Southwest Imports (DSWI) | |
| 4/22/2022 | 27YGI09SALSA | Division of Southwest Imports (DSWI) | |
| 11/7/2018 | 27YGI09SALSA | Division of Southwest Imports (DSWI) | |
| 11/7/2018 | 27YGI09SALSA | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Procesos La Querendona S.A. de C.V.'s FDA import refusal history?
Procesos La Querendona S.A. de C.V. (FEI: 3012304879) has 8 FDA import refusal record(s) in our database, spanning from 11/7/2018 to 11/19/2024.
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. Procesos La Querendona S.A. de C.V.'s FEI number is 3012304879.
What types of violations has Procesos La Querendona S.A. de C.V. received?
Procesos La Querendona S.A. de C.V. 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 Procesos La Querendona S.A. de C.V. come from?
All FDA import refusal data for Procesos La Querendona 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.