Neoventa Medical AB

Form 483

Molndal, -, SwedenFEI 3005011303Issued February 10, 2011

View FDA's Record for This Firm

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.

Observations3

Issue DateFebruary 10, 2011

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Neoventa Medical AB
Location: Molndal, -, Sweden
FEI Number: 3005011303
Product Type: Devices
Issue Date: February 10, 2011
Country: Sweden

Inspection History, 2010 to 2011

VAI1

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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Neoventa Medical AB FDA Form 483, Molndal, February 10, 2011