# FDA Inspection 1018345 - LifeLine Software, Inc. - December 14, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/847b0fdf-944e-49f2-888e-8c5053457653
Source feed: FDA_Inspections

> FDA Inspection 1018345 for LifeLine Software, Inc. on December 14, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018345
- Company Name: LifeLine Software, Inc.
- Inspection Date: 2016-12-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1018345 - 2016-12-14](https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/314110ab-9314-4306-9fb8-d493503497fe)
- [FDA Inspection 968610 - 2016-03-15](https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/1d707d25-6263-4654-a312-1879503105c5)
- [FDA Inspection 856452 - 2013-11-21](https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/ff2f791a-2dee-4330-9a35-af982f7b8288)
- [FDA Inspection 856452 - 2013-11-21](https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/57c03aca-3ec6-4147-b932-1a01b5f3bf8a)
- [FDA Inspection 815038 - 2013-01-25](https://www.globalkeysolutions.net/records/fda_inspections/lifeline-software-inc/eb808710-0e04-476a-b2fb-704d5644e272)

Company: https://www.globalkeysolutions.net/companies/lifeline-software-inc/18e17681-eaff-4233-9577-28e934cd3374

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