# Alivecor, Inc. – FDA Inspection, Aug 6, 2015

Source: https://www.keypedia.com/records/fda_inspections/alivecor-inc/e50ccee0-2232-4b6a-a0e2-45adc713b1ac
Source feed: FDA_Inspections

> FDA inspection 937359 of Alivecor, Inc., August 06, 2015. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 937359
- Company Name: Alivecor, Inc.
- Inspection Date: 2015-08-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1121934 - 2018-10-05](https://www.keypedia.com/records/fda_inspections/alivecor-inc/42d223ae-1e9d-41a5-89a9-4704d3fbeb47)

Company: https://www.keypedia.com/companies/alivecor-inc/f001b7aa-3b4f-4ac8-b11f-917d4d00dedf

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