# Planmeca Oy – FDA Inspection, Nov 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/planmeca-oy/c3a6245e-38c7-481d-a263-71050a5a09e7
Source feed: FDA_Inspections

> FDA inspection 1070539 of Planmeca Oy, November 01, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1070539
- Company Name: Planmeca Oy
- Inspection Date: 2018-11-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 839376 - 2013-06-06
- FDA Inspection 617543 - 2009-09-16

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jeffrey-j-thibodeau/62b74030-4aef-400b-8ae2-8bf84712d813)

Company: https://www.keypedia.com/companies/planmeca-oy/3e74b133-96fc-41ff-8824-cadd6eaf19a7

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7