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Laboratorios Vidastevia S.A.

⚠️ Moderate Risk

FEI: 3008920007 • Bogota, Cundinamarca • COLOMBIA

FEI

FEI Number

3008920007

📍

Location

Bogota, Cundinamarca

🇨🇴

Country

COLOMBIA
🏢

Address

Carrera 42b No. 13-94, , Bogota, Cundinamarca, Colombia

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
8/23/2011
Latest Refusal
8/23/2011
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2382×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

Refusal History

DateProductViolationsDivision
8/23/2011
54YBR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
238UNSAFE ADD
Florida District Office (FLA-DO)
8/23/2011
54YBR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
238UNSAFE ADD
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Laboratorios Vidastevia S.A.'s FDA import refusal history?

Laboratorios Vidastevia S.A. (FEI: 3008920007) has 2 FDA import refusal record(s) in our database, spanning from 8/23/2011 to 8/23/2011.

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. Laboratorios Vidastevia S.A.'s FEI number is 3008920007.

What types of violations has Laboratorios Vidastevia S.A. received?

Laboratorios Vidastevia S.A. 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 Laboratorios Vidastevia S.A. come from?

All FDA import refusal data for Laboratorios Vidastevia S.A. 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.