FDA Inspection 617543 - Planmeca Oy - September 16, 2009

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

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Record Summary

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

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Record Information

Company

Planmeca Oy

Inspection Date

September 16, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6ddfdeb-b4c7-4dca-8c55-47ef59825dc9

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