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Reitex S R L

⚠️ Moderate Risk

FEI: 3004831016 • Vicenza, Vicenza • ITALY

FEI

FEI Number

3004831016

📍

Location

Vicenza, Vicenza

🇮🇹

Country

ITALY
🏢

Address

Via Dell'Edilizia 110, , Vicenza, Vicenza, Italy

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
11/8/2005
Latest Refusal
3/28/2005
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

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).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

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
11/8/2005
76LYBLASER, DENTAL
118NOT LISTED
508NO 510(K)
New York District Office (NYK-DO)
3/28/2005
95L22LASER PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Reitex S R L's FDA import refusal history?

Reitex S R L (FEI: 3004831016) has 2 FDA import refusal record(s) in our database, spanning from 3/28/2005 to 11/8/2005.

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. Reitex S R L's FEI number is 3004831016.

What types of violations has Reitex S R L received?

Reitex S R L has been cited for 3 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 Reitex S R L come from?

All FDA import refusal data for Reitex S R L 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.