# FDA Inspection 1028574 - Encompass Group, LLC - October 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/encompass-group-llc/04a4ce7d-0265-43a9-b235-57bc69d5d8e2
Source feed: FDA_Inspections

> FDA Inspection 1028574 for Encompass Group, LLC on October 12, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028574
- Company Name: Encompass Group, LLC
- Inspection Date: 2017-10-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1028574 - 2017-10-12](https://www.keypedia.com/records/fda_inspections/encompass-group-llc/8344e236-be6c-44e4-9e99-8bbe346a1ef3)

Company: https://www.keypedia.com/companies/encompass-group-llc/ba1c8f63-1a33-4aeb-8de4-da2cafb52d8f

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