# FDA Inspection 1098593 - DyAnsys, Inc - July 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/dyansys-inc/cedeba75-0467-4013-acd6-47691dffd4ac
Source feed: FDA_Inspections

> FDA Inspection 1098593 for DyAnsys, Inc on July 31, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098593
- Company Name: DyAnsys, Inc
- Inspection Date: 2019-07-31
- 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 1098593 - 2019-07-31](https://www.keypedia.com/records/fda_inspections/dyansys-inc/463ff0bf-9fff-45b6-a207-5f9892590dab)

Company: https://www.keypedia.com/companies/dyansys-inc/9506bbfe-c418-47cb-9aeb-782296334bf9

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