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SENSOGRAM TECHNOLOGIES AG

⚠️ Moderate Risk

FEI: 3013340154 • Biel/Bienne, Bern • SWITZERLAND

FEI

FEI Number

3013340154

📍

Location

Biel/Bienne, Bern

🇨🇭
🏢

Address

Ernst-Schuler-Strasse 5, , Biel/Bienne, Bern, Switzerland

Moderate Risk

FDA Import Risk Assessment

25.5
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
7/20/2018
Latest Refusal
5/30/2017
Earliest Refusal

Score Breakdown

Violation Severity
46.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
17.6×10%
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

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

5081×

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
7/20/2018
74PGJOXIMETER, WELLNESS
118NOT LISTED
341REGISTERED
Division of Southeast Imports (DSEI)
5/30/2017
73DQAOXIMETER
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SENSOGRAM TECHNOLOGIES AG's FDA import refusal history?

SENSOGRAM TECHNOLOGIES AG (FEI: 3013340154) has 2 FDA import refusal record(s) in our database, spanning from 5/30/2017 to 7/20/2018.

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. SENSOGRAM TECHNOLOGIES AG's FEI number is 3013340154.

What types of violations has SENSOGRAM TECHNOLOGIES AG received?

SENSOGRAM TECHNOLOGIES AG has been cited for 4 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 SENSOGRAM TECHNOLOGIES AG come from?

All FDA import refusal data for SENSOGRAM TECHNOLOGIES AG 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.