AGROPECUARIA LA DURAZNILLA SPR DE RL
✅ Low Risk
FEI: 3007116915 • Hermosillo, Sonora • MEXICO
FEI Number
3007116915
Location
Hermosillo, Sonora
Country
MEXICOAddress
De La Plata No. 151-A., Col. Parque Industrial, Hermosillo, Sonora, Mexico
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
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.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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.
LIST INGRE
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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
LACKS FIRM
The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/8/2010 | 20RGT06PRICKLE PEAR CACTUS - EDIBLE STEMS OR PADS (CORE FRUIT JAM/JELLY CANDIED), CORE FRUIT JAMS, JELLIES, | Southwest Import District Office (SWI-DO) | |
| 7/8/2010 | 50LGT09CARAMEL | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is AGROPECUARIA LA DURAZNILLA SPR DE RL's FDA import refusal history?
AGROPECUARIA LA DURAZNILLA SPR DE RL (FEI: 3007116915) has 2 FDA import refusal record(s) in our database, spanning from 7/8/2010 to 7/8/2010.
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. AGROPECUARIA LA DURAZNILLA SPR DE RL's FEI number is 3007116915.
What types of violations has AGROPECUARIA LA DURAZNILLA SPR DE RL received?
AGROPECUARIA LA DURAZNILLA SPR DE RL has been cited for 7 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 AGROPECUARIA LA DURAZNILLA SPR DE RL come from?
All FDA import refusal data for AGROPECUARIA LA DURAZNILLA SPR DE RL 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.