# FDA Inspection 957619 - Alertwatch, Inc. - February 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/alertwatch-inc/b0ee84c2-4403-4ba6-93ff-5a7fbf8b5bea
Source feed: FDA_Inspections

> FDA Inspection 957619 for Alertwatch, Inc. on February 04, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 957619
- Company Name: Alertwatch, Inc.
- Inspection Date: 2016-02-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 957619 - 2016-02-04](https://www.keypedia.com/records/fda_inspections/alertwatch-inc/0744a27b-56e1-44ae-8885-91757bbc24bd)

Company: https://www.keypedia.com/companies/alertwatch-inc/ad0313d9-ea0f-4634-b814-d959501ac95b

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