# FDA Inspection 1089893 - EHOB, Inc. - May 06, 2019

Source: https://www.keypedia.com/records/fda_inspections/ehob-inc/85ba8d8a-67f5-47bf-857e-eeade40b05d2
Source feed: FDA_Inspections

> FDA Inspection 1089893 for EHOB, Inc. on May 06, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089893
- Company Name: EHOB, Inc.
- Inspection Date: 2019-05-06
- 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 1089893 - 2019-05-06](https://www.keypedia.com/records/fda_inspections/ehob-inc/a5d32271-bb43-491e-9745-dc1121d5e964)

Company: https://www.keypedia.com/companies/ehob-inc/24c28d3b-ade2-4a93-a4a9-ef7570c34a03

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