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Planmeca Oy

✅ Low Risk

FEI: 1000207287 • Helsinki, Uusimaa • FINLAND

FEI

FEI Number

1000207287

📍

Location

Helsinki, Uusimaa

🇫🇮

Country

FINLAND
🏢

Address

Asentajankatu 6, , Helsinki, Uusimaa, Finland

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
4/10/2017
Latest Refusal
4/10/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
4/10/2017
90MQBSOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Planmeca Oy's FDA import refusal history?

Planmeca Oy (FEI: 1000207287) has 1 FDA import refusal record(s) in our database, spanning from 4/10/2017 to 4/10/2017.

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. Planmeca Oy's FEI number is 1000207287.

What types of violations has Planmeca Oy received?

Planmeca Oy 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 Planmeca Oy come from?

All FDA import refusal data for Planmeca Oy 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.