# FDA Inspection 1180656 - Relievant Medsystems, Inc. - June 23, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/relievant-medsystems-inc/df2000cd-5129-47bf-8465-484ab5673b35
Source feed: FDA_Inspections

> FDA Inspection 1180656 for Relievant Medsystems, Inc. on June 23, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180656
- Company Name: Relievant Medsystems, Inc.
- Inspection Date: 2022-06-23
- 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 1180656 - 2022-06-23](https://www.globalkeysolutions.net/records/fda_inspections/relievant-medsystems-inc/d1532430-e705-4141-b496-4b236cbf4c4a)
- [FDA Inspection 1040049 - 2018-01-26](https://www.globalkeysolutions.net/records/fda_inspections/relievant-medsystems-inc/fbc94b2a-4213-411e-bcc2-3f0fd64768b4)
- [FDA Inspection 909309 - 2014-12-19](https://www.globalkeysolutions.net/records/fda_inspections/relievant-medsystems-inc/ea07ad1b-c61b-4257-a5bd-15518dbd0f41)

Company: https://www.globalkeysolutions.net/companies/relievant-medsystems-inc/d2a5ef34-1737-454d-9c1d-0155ca400c52

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