# Alertwatch, Inc. – FDA Inspection, Feb 4, 2016

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

> FDA inspection 957619 of Alertwatch, Inc., February 04, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

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