# FDA Inspection 920789 - NeoSoft, LLC - March 31, 2015

Source: https://www.keypedia.com/records/fda_inspections/neosoft-llc/f1c156a4-954e-4274-bb34-5b00695d0e5e
Source feed: FDA_Inspections

> FDA Inspection 920789 for NeoSoft, LLC on March 31, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920789
- Company Name: NeoSoft, LLC
- Inspection Date: 2015-03-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 920789 - 2015-03-31](https://www.keypedia.com/records/fda_inspections/neosoft-llc/666e6dd4-9e4b-4267-bcf3-11cd5f252200)

Company: https://www.keypedia.com/companies/neosoft-llc/6e8efd55-51f3-4811-9bf1-14384b656434

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