# Exergen Corporation – FDA Inspection, Jan 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/exergen-corporation/cfec5803-744d-4e1b-a22e-63eb839b40c1
Source feed: FDA_Inspections

> FDA inspection 997742 of Exergen Corporation, January 19, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997742
- Company Name: Exergen Corporation
- Inspection Date: 2017-01-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 780129 - 2012-05-03
- FDA Inspection 568583 - 2009-02-19

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)

Company: https://www.keypedia.com/companies/exergen-corporation/793a7afe-05f2-4e66-8efd-977ec77c7f98

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