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Flextronics Manufacturing Europe Bv

⚠️ Moderate Risk

FEI: 3007021214 • Timisoaratimisoara • ROMANIA

FEI

FEI Number

3007021214

📍

Location

Timisoaratimisoara

🇷🇴

Country

ROMANIA
🏢

Address

Calea Torontalului Dn 6 Km 5,7c/O Wmt, , Timisoaratimisoara, , Romania

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
10/26/2010
Latest Refusal
10/26/2010
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

1182×

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
10/26/2010
74MHXMONITOR, PHYSIOLOGICAL, PATIENT
118NOT LISTED
New York District Office (NYK-DO)
10/26/2010
74DSIDETECTOR AND ALARM, ARRHYTHMIA
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Flextronics Manufacturing Europe Bv's FDA import refusal history?

Flextronics Manufacturing Europe Bv (FEI: 3007021214) has 2 FDA import refusal record(s) in our database, spanning from 10/26/2010 to 10/26/2010.

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. Flextronics Manufacturing Europe Bv's FEI number is 3007021214.

What types of violations has Flextronics Manufacturing Europe Bv received?

Flextronics Manufacturing Europe Bv has been cited for 1 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 Flextronics Manufacturing Europe Bv come from?

All FDA import refusal data for Flextronics Manufacturing Europe Bv 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.