# FDA Inspection 1087836 - HHS Systems Inc. - April 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/hhs-systems-inc/56f43e30-3a3b-4fb0-801a-07851e8a46ec
Source feed: FDA_Inspections

> FDA Inspection 1087836 for HHS Systems Inc. on April 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087836
- Company Name: HHS Systems Inc.
- Inspection Date: 2019-04-25
- 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 1168648 - 2022-03-18](https://www.globalkeysolutions.net/records/fda_inspections/hhs-systems-inc/fdfe2b7e-bbfe-4d11-9798-c7f3e07b362d)
- [FDA Inspection 1087836 - 2019-04-25](https://www.globalkeysolutions.net/records/fda_inspections/hhs-systems-inc/b1790dd3-a467-4130-859f-ffbc2949db6c)

Company: https://www.globalkeysolutions.net/companies/hhs-systems-inc/9f78510a-2095-44a5-b1ac-0611cd8d32ad

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