# FDA Inspection 1085854 - Trimedyne Inc - March 21, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/trimedyne-inc/2e3619bc-aad9-4d70-83ca-06462821407b
Source feed: FDA_Inspections

> FDA Inspection 1085854 for Trimedyne Inc on March 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085854
- Company Name: Trimedyne Inc
- Inspection Date: 2019-03-21
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 983196 - 2016-08-25](https://www.globalkeysolutions.net/records/fda_inspections/trimedyne-inc/1a8c86a0-2ae9-4987-896b-b27502f2d239)
- [FDA Inspection 735632 - 2011-07-22](https://www.globalkeysolutions.net/records/fda_inspections/trimedyne-inc/455f686b-a617-4870-b767-74940b4a15f2)
- [FDA Inspection 735632 - 2011-07-22](https://www.globalkeysolutions.net/records/fda_inspections/trimedyne-inc/5a3942da-5050-40ba-8824-f2c73ac39455)
- [FDA Inspection 735632 - 2011-07-22](https://www.globalkeysolutions.net/records/fda_inspections/trimedyne-inc/bd935a06-af76-4b88-915f-0e862c264050)

Company: https://www.globalkeysolutions.net/companies/trimedyne-inc/183dcae3-5ed5-4330-af52-ad7aeefcbe04

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