# FDA Inspection 1020357 - Lifeline Systems Company - August 04, 2017

Source: https://www.keypedia.com/records/fda_inspections/lifeline-systems-company/2ded463c-5880-45aa-96f8-033b983f84f3
Source feed: FDA_Inspections

> FDA Inspection 1020357 for Lifeline Systems Company on August 04, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020357
- Company Name: Lifeline Systems Company
- Inspection Date: 2017-08-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/lifeline-systems-company/a48afeee-ddbc-416b-8079-0f920d732d41

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