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HECHO EN MEXICO POR TECHOFORMA S

⚠️ Moderate Risk

FEI: 3023461095 • San Juan Del Rio Quer • MEXICO

FEI

FEI Number

3023461095

📍

Location

San Juan Del Rio Quer

🇲🇽

Country

MEXICO
🏢

Address

Oriente 10no 8 Col Nuev, , San Juan Del Rio Quer, , Mexico

Moderate Risk

FDA Import Risk Assessment

36.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/1/2022
Latest Refusal
9/1/2022
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
18.7×20%
Frequency
10.0×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
9/1/2022
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HECHO EN MEXICO POR TECHOFORMA S's FDA import refusal history?

HECHO EN MEXICO POR TECHOFORMA S (FEI: 3023461095) has 1 FDA import refusal record(s) in our database, spanning from 9/1/2022 to 9/1/2022.

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. HECHO EN MEXICO POR TECHOFORMA S's FEI number is 3023461095.

What types of violations has HECHO EN MEXICO POR TECHOFORMA S received?

HECHO EN MEXICO POR TECHOFORMA S has been cited for 2 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 HECHO EN MEXICO POR TECHOFORMA S come from?

All FDA import refusal data for HECHO EN MEXICO POR TECHOFORMA S 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.