# Neoventa Medical AB – FDA Inspection, Apr 1, 2010

Source: https://www.keypedia.com/records/fda_inspections/neoventa-medical-ab/863ee3e7-8abf-4a0a-af4f-1851dff22ce4
Source feed: FDA_Inspections

> FDA inspection 658312 of Neoventa Medical AB, April 01, 2010. Classification: Official Action Indicated (OAI). 7 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 658312
- Company Name: Neoventa Medical AB
- Inspection Date: 2010-04-01
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 709564 - 2011-02-10

Company: https://www.keypedia.com/companies/neoventa-medical-ab/1f21c969-6c75-4fed-aebb-de581adc2e4e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7