# Thermotek, Inc. – FDA Inspection, Jul 22, 2016

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

> FDA inspection 981384 of Thermotek, Inc., July 22, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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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)
- 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

## Related Documents

- FDA Inspection 855517 - 2013-11-06
- FDA Inspection 677403 - 2010-08-25

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