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VITAE LABORATORIOS SA DE CV

⚠️ Moderate Risk

FEI: 3025345323 • Jalisco • MEXICO

FEI

FEI Number

3025345323

📍

Location

Jalisco

🇲🇽

Country

MEXICO
🏢

Address

Calle Paseo Del Valle N, , Jalisco, , Mexico

Moderate Risk

FDA Import Risk Assessment

37.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/10/2023
Latest Refusal
1/10/2023
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
25.9×20%
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
1/10/2023
64HCA99EXPECTORANT N.E.C.
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is VITAE LABORATORIOS SA DE CV's FDA import refusal history?

VITAE LABORATORIOS SA DE CV (FEI: 3025345323) has 1 FDA import refusal record(s) in our database, spanning from 1/10/2023 to 1/10/2023.

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. VITAE LABORATORIOS SA DE CV's FEI number is 3025345323.

What types of violations has VITAE LABORATORIOS SA DE CV received?

VITAE LABORATORIOS SA DE CV 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 VITAE LABORATORIOS SA DE CV come from?

All FDA import refusal data for VITAE LABORATORIOS SA DE CV 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.