ImportRefusal LogoImportRefusal

Ferrari Spa-Es.Fabbr.Autom.E Corse

⚠️ Moderate Risk

FEI: 1000373939 • Modena, Modena • ITALY

FEI

FEI Number

1000373939

📍

Location

Modena, Modena

🇮🇹

Country

ITALY
🏢

Address

Via Emilia Est 1163, , Modena, Modena, Italy

Moderate Risk

FDA Import Risk Assessment

27.4
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
8/30/2013
Latest Refusal
1/31/2013
Earliest Refusal

Score Breakdown

Violation Severity
44.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3413×

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).

1182×

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).

2311×

LENS CERT

The lenses are declared by accompanying certificate to meet the requirements for impact-resistant lenses in 21 CFR 801.410 but does not appear to be impact-resistant.

2351×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

Refusal History

DateProductViolationsDivision
8/30/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
341REGISTERED
Florida District Office (FLA-DO)
1/31/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
341REGISTERED
New York District Office (NYK-DO)
1/31/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
231LENS CERT
341REGISTERED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Ferrari Spa-Es.Fabbr.Autom.E Corse's FDA import refusal history?

Ferrari Spa-Es.Fabbr.Autom.E Corse (FEI: 1000373939) has 3 FDA import refusal record(s) in our database, spanning from 1/31/2013 to 8/30/2013.

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. Ferrari Spa-Es.Fabbr.Autom.E Corse's FEI number is 1000373939.

What types of violations has Ferrari Spa-Es.Fabbr.Autom.E Corse received?

Ferrari Spa-Es.Fabbr.Autom.E Corse 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 Ferrari Spa-Es.Fabbr.Autom.E Corse come from?

All FDA import refusal data for Ferrari Spa-Es.Fabbr.Autom.E Corse 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.