# FDA Inspection 1118136 - Retia  Medical Systems Inc - December 02, 2019

Source: https://www.keypedia.com/records/fda_inspections/retia-medical-systems-inc/a4155f8e-eaf8-44d5-a93e-dedd9f8f4d20
Source feed: FDA_Inspections

> FDA Inspection 1118136 for Retia  Medical Systems Inc on December 02, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1118136
- Company Name: Retia  Medical Systems Inc
- Inspection Date: 2019-12-02
- Classification: No Action Indicated (NAI)
- 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/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