FDA Inspection 1070539 - Planmeca Oy - November 01, 2018

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Record Details

This FDA Inspection record concerns Planmeca Oy, with an inspection on November 1, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Planmeca Oy
Inspection Date: November 1, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4c1608f4-f569-4379-8178-500c236e78ae

Violation Codes6

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(c)21 CFR 820.30(g)21 CFR 820.70(i)21 CFR 820.80(e)

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