# FDA Inspection 549629 - Inditherm Medical - October 30, 2008

Source: https://www.keypedia.com/records/fda_inspections/inditherm-medical/b8162ad2-3a67-422c-a700-4e265cc0b61a
Source feed: FDA_Inspections

> FDA Inspection 549629 for Inditherm Medical on October 30, 2008. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 549629
- Company Name: Inditherm Medical
- Inspection Date: 2008-10-30
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 665536 - 2010-04-29](https://www.keypedia.com/records/fda_inspections/inditherm-medical/95f69e1a-0e9f-4ab3-bb2c-fc55b9bc2a19)
- [FDA Inspection 665536 - 2010-04-29](https://www.keypedia.com/records/fda_inspections/inditherm-medical/b1848241-d314-412d-8b55-492af6b34207)
- [FDA Inspection 549629 - 2008-10-30](https://www.keypedia.com/records/fda_inspections/inditherm-medical/af579fe4-5184-4c02-a690-870306e4e0aa)

Company: https://www.keypedia.com/companies/inditherm-medical/40b5ff40-d13a-4d48-a446-cd07287d3261

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