# FDA Inspection 965132 - InvisionHeart, Inc. - March 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/invisionheart-inc/e9d5a00b-b012-4b12-a519-76eeb1f2be39
Source feed: FDA_Inspections

> FDA Inspection 965132 for InvisionHeart, Inc. on March 31, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965132
- Company Name: InvisionHeart, Inc.
- Inspection Date: 2016-03-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 965132 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/invisionheart-inc/278babb5-dd4b-43ee-964d-9cd3e9d87289)

Company: https://www.keypedia.com/companies/invisionheart-inc/b7784686-dc7d-4d3e-9d79-8115c65c9dc0

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