# DyAnsys, Inc – FDA Inspection, Jul 31, 2019

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

> FDA inspection 1098593 of DyAnsys, Inc, July 31, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

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