Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000207287.
Observations4
Issue DateJune 06, 2013
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Planmeca Oy
Location
Helsinki, -, Finland
FEI Number
1000207287
Product Type
Devices
Issue Date
June 06, 2013
Country
Finland
Inspection History, 2009 to 2018
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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