# FDA Inspection 1053769 - Meditherm Inc. - May 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/meditherm-inc/b650d7e0-4031-40bd-9fa5-05b0c29485c0
Source feed: FDA_Inspections

> FDA Inspection 1053769 for Meditherm Inc. on May 30, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053769
- Company Name: Meditherm Inc.
- Inspection Date: 2018-05-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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