# FDA Inspection 1254008 - Poiesis Medical, LLC - October 30, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/poiesis-medical-llc/5dfbcb91-d0cc-4128-a26c-23e5a0692142/
Source feed: FDA_Inspections

> FDA Inspection 1254008 for Poiesis Medical, LLC on October 30, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1254008
- Company Name: Poiesis Medical, LLC
- Inspection Date: 2024-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1254008 - 2024-10-30](https://www.globalkeysolutions.net/api/records/fda_inspections/poiesis-medical-llc/f68f2e42-c5ce-47d5-afe3-e4bd7a54151d/)
- [FDA Inspection 1254008 - 2024-10-30](https://www.globalkeysolutions.net/api/records/fda_inspections/poiesis-medical-llc/e08ab7be-f8a3-46b2-8013-b8b36785371d/)
- [FDA Inspection 1254008 - 2024-10-30](https://www.globalkeysolutions.net/api/records/fda_inspections/poiesis-medical-llc/a50add3c-61c5-4ce3-9605-59e5f9433201/)
- [FDA Inspection 1078304 - 2019-01-30](https://www.globalkeysolutions.net/api/records/fda_inspections/poiesis-medical-llc/4db80530-3ed4-4dd9-b360-5c8404ddb785/)
- [FDA Inspection 1078304 - 2019-01-30](https://www.globalkeysolutions.net/api/records/fda_inspections/poiesis-medical-llc/55c4dfb4-11dc-4c1b-a172-90d8e28f41e4/)

Company: https://www.globalkeysolutions.net/companies/poiesis-medical-llc/03a8a2d5-3e29-45b1-9b42-c9df9d88ca8e

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