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 3005011303.
Observations7
Issue DateApril 01, 2010
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Neoventa Medical AB
Location
Molndal, -, Sweden
FEI Number
3005011303
Product Type
Devices
Issue Date
April 01, 2010
Country
Sweden
Inspection History, 2010 to 2011
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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