# FDA Inspection 1203388 - Nuwellis Inc - April 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/nuwellis-inc/e6ca2007-9221-4e21-8101-b2b3cf1a06dd
Source feed: FDA_Inspections

> FDA Inspection 1203388 for Nuwellis Inc on April 13, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1203388
- Company Name: Nuwellis Inc
- Inspection Date: 2023-04-13
- 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 1203388 - 2023-04-13](https://www.keypedia.com/records/fda_inspections/nuwellis-inc/d33e3b55-cbc5-4869-8503-e3fa724745a4)
- [FDA Inspection 1005020 - 2016-12-06](https://www.keypedia.com/records/fda_inspections/nuwellis-inc/43f378bb-4b66-466d-808e-ff8ec87634f5)

Company: https://www.keypedia.com/companies/nuwellis-inc/eb4a5877-ef4b-4ff5-ac5a-6b03245b4777

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