# FDA Inspection 1191280 - Retia  Medical Systems Inc - October 14, 2022

Source: https://www.keypedia.com/records/fda_inspections/retia-medical-systems-inc/7f18ad16-e34c-4b34-8a5e-3fa6838762e7
Source feed: FDA_Inspections

> FDA Inspection 1191280 for Retia  Medical Systems Inc on October 14, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1191280
- Company Name: Retia  Medical Systems Inc
- Inspection Date: 2022-10-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1191280 - 2022-10-14](https://www.keypedia.com/records/fda_inspections/retia-medical-systems-inc/b8b48899-c8bb-432e-b135-524d38f3c93e)
- [FDA Inspection 1118136 - 2019-12-02](https://www.keypedia.com/records/fda_inspections/retia-medical-systems-inc/a36b0fa7-08d0-472b-8260-14369bd62634)
- [FDA Inspection 1118136 - 2019-12-02](https://www.keypedia.com/records/fda_inspections/retia-medical-systems-inc/a4155f8e-eaf8-44d5-a93e-dedd9f8f4d20)

Company: https://www.keypedia.com/companies/retia-medical-systems-inc/5e578a1a-3009-45fb-8a9e-15c1a858381c

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