GRUPO GIELPEH SPR DE RI
⚠️ Moderate Risk
FEI: 3010241163 • Quecholac, Puebla • MEXICO
FEI Number
3010241163
Location
Quecholac, Puebla
Country
MEXICOAddress
Camino Nacional No. 302 Francisco I. Madero, , Quecholac, Puebla, 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
LACKS FIRM
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(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/5/2024 | 24TFC11CELERY (LEAF & STEM VEGETABLE) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 10/27/2021 | 24TFC11CELERY (LEAF & STEM VEGETABLE) | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 3/15/2017 | 24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Division of Southwest Imports (DSWI) | |
| 3/15/2017 | 24FFC06SQUASH, SUMMER (FRUIT USED AS VEGETABLE) | Division of Southwest Imports (DSWI) | |
| 3/15/2017 | 25JGB04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE) | Division of Southwest Imports (DSWI) | |
| 3/1/2017 | 24TFC46CILANTRO (LEAF & STEM VEGETABLE) | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is GRUPO GIELPEH SPR DE RI's FDA import refusal history?
GRUPO GIELPEH SPR DE RI (FEI: 3010241163) has 6 FDA import refusal record(s) in our database, spanning from 3/1/2017 to 6/5/2024.
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. GRUPO GIELPEH SPR DE RI's FEI number is 3010241163.
What types of violations has GRUPO GIELPEH SPR DE RI received?
GRUPO GIELPEH SPR DE RI 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 GRUPO GIELPEH SPR DE RI come from?
All FDA import refusal data for GRUPO GIELPEH SPR DE RI 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.