FDA Inspection
LifeLine Software, Inc.LifeLine Software, Inc. – FDA Inspection, Jan 25, 2013
Record Details
This FDA Inspection record concerns LifeLine Software, Inc., with an inspection on January 25, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LifeLine Software, Inc.
- Inspection Date
- January 25, 2013
- Product Type
- Devices
View Company Profile
ID · eb808710-0e04-476a-b2fb-704d5644e272
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 815038
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 806.10(a)(1)Report of risk to health
- 21 CFR 820.30(j)Design history file
Full citation text and observation details available on the Dashboard.
Other FDA inspections of LifeLine Software, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 14, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 15, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 21, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 9, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 20, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for LifeLine Software, Inc.
- 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
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