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Maco International

✅ Low Risk

FEI: 3008002199 • Buccino, Salerno • ITALY

FEI

FEI Number

3008002199

📍

Location

Buccino, Salerno

🇮🇹

Country

ITALY
🏢

Address

Svincolo Buccino 15, LOT, Buccino, Salerno, Italy

Low Risk

FDA Import Risk Assessment

22.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/20/2010
Latest Refusal
8/20/2010
Earliest Refusal

Score Breakdown

Violation Severity
36.7×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

3412×

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).

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).

Refusal History

DateProductViolationsDivision
10/20/2010
76DZDTUBE, ORTHODONTIC
341REGISTERED
Southwest Import District Office (SWI-DO)
8/20/2010
76DZLSCREW, FIXATION, INTRAOSSEOUS
118NOT LISTED
341REGISTERED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Maco International's FDA import refusal history?

Maco International (FEI: 3008002199) has 2 FDA import refusal record(s) in our database, spanning from 8/20/2010 to 10/20/2010.

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. Maco International's FEI number is 3008002199.

What types of violations has Maco International received?

Maco International has been cited for 2 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 Maco International come from?

All FDA import refusal data for Maco International 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.