# FDA Inspection 1070539 - Planmeca Oy - November 01, 2018

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

> FDA Inspection 1070539 for Planmeca Oy on November 01, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1070539 - 2018-11-01](https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/4c1608f4-f569-4379-8178-500c236e78ae)
- [FDA Inspection 1070539 - 2018-11-01](https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/af80c31a-daf0-4be8-9d9f-0db29fb0cb2e)
- [FDA Inspection 839376 - 2013-06-06](https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/73a24f1e-0658-4ad8-9723-41c6154265a1)
- [FDA Inspection 839376 - 2013-06-06](https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/8635b381-afbf-492a-ac74-d322bd072b32)
- [FDA Inspection 839376 - 2013-06-06](https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/84a7ec0b-dc72-4f30-ba66-aa1d466999b8)

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

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