# FDA Inspection 909353 - VentriPoint, Inc. - January 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/ventripoint-inc/77d56d62-ac5c-4a4b-aa50-8bbf537fc17a
Source feed: FDA_Inspections

> FDA Inspection 909353 for VentriPoint, Inc. on January 08, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909353
- Company Name: VentriPoint, Inc.
- Inspection Date: 2015-01-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 909353 - 2015-01-08](https://www.keypedia.com/records/fda_inspections/ventripoint-inc/199ce62c-4330-4b18-a1db-cc2e5fedbdc2)

Company: https://www.keypedia.com/companies/ventripoint-inc/d0dd2b24-9cb8-4501-9423-f84d398ee582

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