# FDA Inspection 981384 - Thermotek, Inc. - July 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/thermotek-inc/eecfba9c-da3a-4b2c-b09a-e87fa910dd98
Source feed: FDA_Inspections

> FDA Inspection 981384 for Thermotek, Inc. on July 22, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981384
- Company Name: Thermotek, Inc.
- Inspection Date: 2016-07-22
- 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 981384 - 2016-07-22](https://www.keypedia.com/records/fda_inspections/thermotek-inc/d6ca685e-17e0-4855-8095-25ba5058f6a7)
- [FDA Inspection 855517 - 2013-11-06](https://www.keypedia.com/records/fda_inspections/thermotek-inc/930baaf9-3391-4f94-a6da-76c4203b4659)
- [FDA Inspection 855517 - 2013-11-06](https://www.keypedia.com/records/fda_inspections/thermotek-inc/16b033bd-9741-4e7b-b295-387dec5bed67)
- [FDA Inspection 677403 - 2010-08-25](https://www.keypedia.com/records/fda_inspections/thermotek-inc/e5213aaf-7fa4-4afc-9e0b-b682b1508697)
- [FDA Inspection 677403 - 2010-08-25](https://www.keypedia.com/records/fda_inspections/thermotek-inc/d3e1eb4c-24aa-4a87-8ab6-63b14b3636b2)

Company: https://www.keypedia.com/companies/thermotek-inc/55b779e1-6bed-4acc-b7bd-ae0eb22500be

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