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Lanificio F.Lli Cerruti Spa

⚠️ Moderate Risk

FEI: 3010247596 • Biella, Bi • ITALY

FEI

FEI Number

3010247596

📍

Location

Biella, Bi

🇮🇹

Country

ITALY
🏢

Address

Via Cernaia, 40, , Biella, Bi, Italy

Moderate Risk

FDA Import Risk Assessment

30.4
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
7/3/2013
Latest Refusal
7/3/2013
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2354×

NOT IMPACT

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

32804×

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.

37414×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

Refusal History

DateProductViolationsDivision
7/3/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
7/3/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
7/3/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)
7/3/2013
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
235NOT IMPACT
3280FRNMFGREG
3741FRNMFGREG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Lanificio F.Lli Cerruti Spa's FDA import refusal history?

Lanificio F.Lli Cerruti Spa (FEI: 3010247596) has 4 FDA import refusal record(s) in our database, spanning from 7/3/2013 to 7/3/2013.

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. Lanificio F.Lli Cerruti Spa's FEI number is 3010247596.

What types of violations has Lanificio F.Lli Cerruti Spa received?

Lanificio F.Lli Cerruti 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 Lanificio F.Lli Cerruti Spa come from?

All FDA import refusal data for Lanificio F.Lli Cerruti 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.