# FDA Inspection 937359 - Alivecor, Inc. - August 06, 2015

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

> FDA Inspection 937359 for Alivecor, Inc. on August 06, 2015. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 937359 - 2015-08-06](https://www.keypedia.com/records/fda_inspections/alivecor-inc/cc349f34-f752-4d9e-9237-46ec63d092ce)

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