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BIOSYNEX SWISS S.A

⚠️ Moderate Risk

FEI: 3016727137 • Fribourg, Fribourg • SWITZERLAND

FEI

FEI Number

3016727137

📍

Location

Fribourg, Fribourg

🇨🇭
🏢

Address

Rue De Romont 29-31, , Fribourg, Fribourg, Switzerland

Moderate Risk

FDA Import Risk Assessment

37.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/31/2021
Latest Refusal
7/22/2020
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
27.0×10%
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

5083×

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
8/31/2021
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
508NO 510(K)
Division of Southeast Imports (DSEI)
8/31/2021
83QOFMULTI-TARGET RESPIRATORY SPECIMEN NUCLEIC ACID TEST INCLUDING SARS-COV-2 AND OTHER MICROBIAL AGENTS
508NO 510(K)
Division of Southeast Imports (DSEI)
7/22/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is BIOSYNEX SWISS S.A's FDA import refusal history?

BIOSYNEX SWISS S.A (FEI: 3016727137) has 3 FDA import refusal record(s) in our database, spanning from 7/22/2020 to 8/31/2021.

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. BIOSYNEX SWISS S.A's FEI number is 3016727137.

What types of violations has BIOSYNEX SWISS S.A received?

BIOSYNEX SWISS 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 BIOSYNEX SWISS S.A come from?

All FDA import refusal data for BIOSYNEX SWISS 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.