# LifeLine Software, Inc. – FDA Inspection, Jan 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/lifeline-software-inc/eb808710-0e04-476a-b2fb-704d5644e272
Source feed: FDA_Inspections

> FDA inspection 815038 of LifeLine Software, Inc., January 25, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 806 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 815038
- Company Name: LifeLine Software, Inc.
- Inspection Date: 2013-01-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1018345 - 2016-12-14
- FDA Inspection 968610 - 2016-03-15
- FDA Inspection 856452 - 2013-11-21
- FDA Inspection 729825 - 2011-06-09
- FDA Inspection 657927 - 2010-04-20

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

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