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Cefla s.c.

✅ Low Risk

FEI: 3006610845 • Imola, Bologna • ITALY

FEI

FEI Number

3006610845

📍

Location

Imola, Bologna

🇮🇹

Country

ITALY
🏢

Address

Via Bicocca 14/C, , Imola, Bologna, Italy

Low Risk

FDA Import Risk Assessment

23.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
9/11/2015
Latest Refusal
9/11/2015
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
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).

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).

Refusal History

DateProductViolationsDivision
9/11/2015
90IZLSYSTEM, X-RAY, MOBILE
118NOT LISTED
341REGISTERED
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Cefla s.c.'s FDA import refusal history?

Cefla s.c. (FEI: 3006610845) has 1 FDA import refusal record(s) in our database, spanning from 9/11/2015 to 9/11/2015.

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. Cefla s.c.'s FEI number is 3006610845.

What types of violations has Cefla s.c. received?

Cefla s.c. 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 Cefla s.c. come from?

All FDA import refusal data for Cefla s.c. 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.