# FDA Inspection 997742 - Exergen Corporation - January 19, 2017

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

> FDA Inspection 997742 for Exergen Corporation on January 19, 2017. Classification: Voluntary Action Indicated (VAI).

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

## Related Documents

- [FDA Inspection 780129 - 2012-05-03](https://www.keypedia.com/records/fda_inspections/exergen-corporation/bf41d8b5-a5a7-4a3c-8453-1bfd848411c4)
- [FDA Inspection 568583 - 2009-02-19](https://www.keypedia.com/records/fda_inspections/exergen-corporation/f495341c-cea6-4e0d-aec0-996e68fa2ece)

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