# FDA Inspection 1065486 - Simpro - September 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/simpro/76784703-7bfb-4d91-891e-3b9bd3653ff7
Source feed: FDA_Inspections

> FDA Inspection 1065486 for Simpro on September 13, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065486
- Company Name: Simpro
- Inspection Date: 2018-09-13
- 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 1065486 - 2018-09-13](https://www.globalkeysolutions.net/records/fda_inspections/simpro/ed482aee-0a9c-4a4e-b863-bb487e16fa98)
- [FDA Inspection 976427 - 2016-07-07](https://www.globalkeysolutions.net/records/fda_inspections/simpro/605ca90b-4fce-4f5c-bfbe-1fa495a479ba)

Company: https://www.globalkeysolutions.net/companies/simpro/06ca0275-8d6a-45af-91e3-363e5f6af312

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