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Grupo de Hongo Zeta Endotzi SPR de RL

⚠️ Moderate Risk

FEI: 3010186668 • Jiquipilco, Mexico • MEXICO

FEI

FEI Number

3010186668

📍

Location

Jiquipilco, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Domicilio Conocido Loma De Endotzi, Manzana Sexta S/N; Jiquipilco, Jiquipilco, Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

45.1
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
4
Unique Violations
1/19/2024
Latest Refusal
2/18/2015
Earliest Refusal

Score Breakdown

Violation Severity
62.0×40%
Refusal Volume
25.9×30%
Recency
60.5×20%
Frequency
4.5×10%
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

38982×

INADPRCCTL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health due to inadequate process controls.

3211×

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.

4821×

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.

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
1/19/2024
25RCE99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
3898INADPRCCTL
Division of Southwest Imports (DSWI)
1/19/2024
25RCE99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
3898INADPRCCTL
Division of Southwest Imports (DSWI)
5/25/2016
25PCE15OYSTER MUSHROOMS, WHOLE (BUTTON) (FUNGI)
321LACKS N/C
482NUTRIT LBL
Division of Southwest Imports (DSWI)
2/18/2015
25RGI99MUSHROOMS AND OTHER FUNGI PRODUCTS, BROKEN OR KIBBLED, N.E.C.
83NO PROCESS
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Grupo de Hongo Zeta Endotzi SPR de RL's FDA import refusal history?

Grupo de Hongo Zeta Endotzi SPR de RL (FEI: 3010186668) has 4 FDA import refusal record(s) in our database, spanning from 2/18/2015 to 1/19/2024.

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. Grupo de Hongo Zeta Endotzi SPR de RL's FEI number is 3010186668.

What types of violations has Grupo de Hongo Zeta Endotzi SPR de RL received?

Grupo de Hongo Zeta Endotzi SPR de RL 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 de Hongo Zeta Endotzi SPR de RL come from?

All FDA import refusal data for Grupo de Hongo Zeta Endotzi 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.