# FDA Inspection 840359 - Haas Software - July 10, 2013

Source: https://www.keypedia.com/records/fda_inspections/haas-software/1a588686-7cd3-45c1-a49c-0daae367d36a
Source feed: FDA_Inspections

> FDA Inspection 840359 for Haas Software on July 10, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 840359
- Company Name: Haas Software
- Inspection Date: 2013-07-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 887366 - 2014-07-17](https://www.keypedia.com/records/fda_inspections/haas-software/7b2ea86a-88a3-4ced-bfcb-ea51dbce3077)
- [FDA Inspection 887366 - 2014-07-17](https://www.keypedia.com/records/fda_inspections/haas-software/19605d18-106a-4099-b996-1e8b8a28320c)
- [FDA Inspection 840359 - 2013-07-10](https://www.keypedia.com/records/fda_inspections/haas-software/a8e0d320-f627-4da8-96b6-e25d4300aed5)

Company: https://www.keypedia.com/companies/haas-software/5d84e81d-c557-422f-8505-55ae0c287aa1

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