# FDA Inspection 1038061 - Bio-Thesiometer USA - January 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/bio-thesiometer-usa/91155a6b-7960-41bd-9cdb-64d1ccfe5dea
Source feed: FDA_Inspections

> FDA Inspection 1038061 for Bio-Thesiometer USA on January 19, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038061
- Company Name: Bio-Thesiometer USA
- Inspection Date: 2018-01-19
- 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 1038061 - 2018-01-19](https://www.keypedia.com/records/fda_inspections/bio-thesiometer-usa/ec169c19-f939-4738-b950-a542f6cb0a67)

Company: https://www.keypedia.com/companies/bio-thesiometer-usa/cc92df30-768a-4d6c-a27e-cf5c23a3886c

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