# FDA Inspection 617543 - Planmeca Oy - September 16, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/planmeca-oy/f6ddfdeb-b4c7-4dca-8c55-47ef59825dc9/
Source feed: FDA_Inspections

> FDA Inspection 617543 for Planmeca Oy on September 16, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 617543
- Company Name: Planmeca Oy
- Inspection Date: 2009-09-16
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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