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Veda Lab

⚠️ Moderate Risk

FEI: 3000254998 • Alancon, Cedex • FRANCE

FEI

FEI Number

3000254998

📍

Location

Alancon, Cedex

🇫🇷

Country

FRANCE
🏢

Address

Rue De L'Expansion, , Alancon, Cedex, France

Moderate Risk

FDA Import Risk Assessment

39.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
6/4/2021
Latest Refusal
6/2/2020
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
39.8×10%
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

5084×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
6/4/2021
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Northeast Imports (DNEI)
7/24/2020
82OTRRESEARCH USE ONLY/IMMUNOLOGY DEVICES
508NO 510(K)
Division of Southeast Imports (DSEI)
7/1/2020
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
508NO 510(K)
Division of Southeast Imports (DSEI)
6/2/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Veda Lab's FDA import refusal history?

Veda Lab (FEI: 3000254998) has 4 FDA import refusal record(s) in our database, spanning from 6/2/2020 to 6/4/2021.

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. Veda Lab's FEI number is 3000254998.

What types of violations has Veda Lab received?

Veda Lab 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 Veda Lab come from?

All FDA import refusal data for Veda Lab 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.