# FDA Inspection 935425 - Lifesync Corporation - July 24, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/lifesync-corporation/dadf91af-0cc1-4716-81d0-d8f3557bee17
Source feed: FDA_Inspections

> FDA Inspection 935425 for Lifesync Corporation on July 24, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935425
- Company Name: Lifesync Corporation
- Inspection Date: 2015-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 935425 - 2015-07-24](https://www.globalkeysolutions.net/records/fda_inspections/lifesync-corporation/178b0680-15d3-4809-a13c-846e627b79f8)
- [FDA Inspection 763668 - 2012-01-11](https://www.globalkeysolutions.net/records/fda_inspections/lifesync-corporation/13cc5adc-3f44-4423-87a3-b27b40ebd217)
- [FDA Inspection 763668 - 2012-01-11](https://www.globalkeysolutions.net/records/fda_inspections/lifesync-corporation/79dd193a-a44a-4a29-8fb3-d689b98be1ef)

Company: https://www.globalkeysolutions.net/companies/lifesync-corporation/a5921065-dac5-4b87-a7a3-b4da460bc2c2

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