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DMM Vission, S.A. de C.V.

⚠️ Moderate Risk

FEI: 3016833130 • Ciudad Nezahualcoyotl, Mexico • MEXICO

FEI

FEI Number

3016833130

📍

Location

Ciudad Nezahualcoyotl, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Calle Lago Guija 234, Col. Agua Azul, Nezahualcoyotl, Ciudad Nezahualcoyotl, Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/13/2020
Latest Refusal
10/13/2020
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
10/13/2020
62HBY05ETHYL ALCOHOL (ANTI-MICROBIAL)
27DRUG GMPS
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is DMM Vission, S.A. de C.V.'s FDA import refusal history?

DMM Vission, S.A. de C.V. (FEI: 3016833130) has 1 FDA import refusal record(s) in our database, spanning from 10/13/2020 to 10/13/2020.

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. DMM Vission, S.A. de C.V.'s FEI number is 3016833130.

What types of violations has DMM Vission, S.A. de C.V. received?

DMM Vission, S.A. de C.V. has been cited for 1 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 DMM Vission, S.A. de C.V. come from?

All FDA import refusal data for DMM Vission, 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.