# Gentherm Medical, LLC – FDA Inspection, Jan 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/gentherm-medical-llc/961e54c5-b2db-4dd8-96f2-3c6d38a66383
Source feed: FDA_Inspections

> FDA inspection 1003116 of Gentherm Medical, LLC, January 18, 2017. Classification: No Action Indicated (NAI). 6 citations under 21 CFR part 820. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003116
- Company Name: Gentherm Medical, LLC
- Inspection Date: 2017-01-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1133261 - 2020-10-09](https://www.keypedia.com/records/fda_inspections/gentherm-medical-llc/f7ba705b-c485-4319-81f9-1aa56651499c)
- [FDA Inspection 1063862 - 2018-08-30](https://www.keypedia.com/records/fda_inspections/gentherm-medical-llc/3c36228e-1ebe-489d-b478-1576d8a1dec3)
- [FDA Inspection 1041699 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/gentherm-medical-llc/ab4c6abc-5141-4b58-945b-d63cce6cbfce)
- FDA Inspection 820605 - 2013-03-01
- FDA Inspection 753901 - 2011-11-18

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)
- Teresa K. Kastner

Company: https://www.keypedia.com/companies/gentherm-medical-llc/87f51b22-51ce-42c8-8580-b5fcc27937b6

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