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Multimedical S.R.L.

⚠️ Moderate Risk

FEI: 3005622231 • Viadana, Mantova • ITALY

FEI

FEI Number

3005622231

📍

Location

Viadana, Mantova

🇮🇹

Country

ITALY
🏢

Address

Via Guido Rossa 71, , Viadana, Mantova, Italy

Moderate Risk

FDA Import Risk Assessment

28.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
3/31/2015
Latest Refusal
1/31/2013
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
13.9×10%
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).

27801×

DEVICEGMPS

The article is subject to refusal of admission pursuant to Section 801(a)(1) in that the methods used in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the device do not conform to the requirements of Section 520(f)(1) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) or a condition prescribed by an order under section 520(f)(2) of the FD&C 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
3/31/2015
80MHCPORT, INTRAOSSEOUS, IMPLANTED
118NOT LISTED
Division of Southeast Imports (DSEI)
3/30/2015
80MHCPORT, INTRAOSSEOUS, IMPLANTED
2780DEVICEGMPS
Florida District Office (FLA-DO)
1/31/2013
80KCTSTERILIZATION WRAP CONTAINERS, TRAYS, CASSETTES & OTHER ACCESSORIES
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

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

Multimedical S.R.L. (FEI: 3005622231) has 3 FDA import refusal record(s) in our database, spanning from 1/31/2013 to 3/31/2015.

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. Multimedical S.R.L.'s FEI number is 3005622231.

What types of violations has Multimedical S.R.L. received?

Multimedical 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 Multimedical S.R.L. come from?

All FDA import refusal data for Multimedical 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.