# FDA Inspection 1179170 - Meditherm Inc. - September 02, 2022

Source: https://www.keypedia.com/records/fda_inspections/meditherm-inc/0e539e4c-3b7d-4249-a87d-6afc7b66960a
Source feed: FDA_Inspections

> FDA Inspection 1179170 for Meditherm Inc. on September 02, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179170
- Company Name: Meditherm Inc.
- Inspection Date: 2022-09-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179170 - 2022-09-02](https://www.keypedia.com/records/fda_inspections/meditherm-inc/e79056c6-431c-473a-b467-7081e7faa8b1)
- [FDA Inspection 1053769 - 2018-05-30](https://www.keypedia.com/records/fda_inspections/meditherm-inc/ee3b13fb-f4ab-4646-b469-9322c3a35b81)
- [FDA Inspection 1053769 - 2018-05-30](https://www.keypedia.com/records/fda_inspections/meditherm-inc/b650d7e0-4031-40bd-9fa5-05b0c29485c0)

Company: https://www.keypedia.com/companies/meditherm-inc/ae70b280-688b-4d3f-a407-fa2751f5f9a2

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