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Demetra S.A.S.

⚠️ Moderate Risk

FEI: 3003828909 • Messina, Messina • ITALY

FEI

FEI Number

3003828909

📍

Location

Messina, Messina

🇮🇹

Country

ITALY
🏢

Address

Via Gonfalone 382, , Messina, Messina, Italy

Moderate Risk

FDA Import Risk Assessment

37.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
4/18/2003
Latest Refusal
4/18/2003
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
4/18/2003
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
508NO 510(K)
New Orleans District Office (NOL-DO)
4/18/2003
84LLPLASER FOR PAIN THERAPY
237NO PMA
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Demetra S.A.S.'s FDA import refusal history?

Demetra S.A.S. (FEI: 3003828909) has 2 FDA import refusal record(s) in our database, spanning from 4/18/2003 to 4/18/2003.

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. Demetra S.A.S.'s FEI number is 3003828909.

What types of violations has Demetra S.A.S. received?

Demetra S.A.S. 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 Demetra S.A.S. come from?

All FDA import refusal data for Demetra S.A.S. 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.