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Fondinox Spa

✅ Low Risk

FEI: 3010613957 • Sergnano • ITALY

FEI

FEI Number

3010613957

📍

Location

Sergnano

🇮🇹

Country

ITALY
🏢

Address

Via Ferrante Aportl 18, , Sergnano, , Italy

Low Risk

FDA Import Risk Assessment

21.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
2/24/2014
Latest Refusal
2/24/2014
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
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).

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.

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
2/24/2014
90IWZFILM, RADIOGRAPHIC
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Fondinox Spa's FDA import refusal history?

Fondinox Spa (FEI: 3010613957) has 1 FDA import refusal record(s) in our database, spanning from 2/24/2014 to 2/24/2014.

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. Fondinox Spa's FEI number is 3010613957.

What types of violations has Fondinox Spa received?

Fondinox Spa 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 Fondinox Spa come from?

All FDA import refusal data for Fondinox Spa 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.