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X-Rite Europe Ag

✅ Low Risk

FEI: 3007058733 • Regensdorf, Zurich • SWITZERLAND

FEI

FEI Number

3007058733

📍

Location

Regensdorf, Zurich

🇨🇭
🏢

Address

Althardstrasse 70, , Regensdorf, Zurich, Switzerland

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
8/15/2017
Latest Refusal
8/15/2017
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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).

3411×

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).

Refusal History

DateProductViolationsDivision
8/15/2017
75JJQCOLORIMETER, PHOTOMETER, SPECTROPHOTOMETER FOR CLINICAL USE
118NOT LISTED
341REGISTERED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is X-Rite Europe Ag's FDA import refusal history?

X-Rite Europe Ag (FEI: 3007058733) has 1 FDA import refusal record(s) in our database, spanning from 8/15/2017 to 8/15/2017.

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. X-Rite Europe Ag's FEI number is 3007058733.

What types of violations has X-Rite Europe Ag received?

X-Rite Europe Ag 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 X-Rite Europe Ag come from?

All FDA import refusal data for X-Rite Europe 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.