# FDA Inspection 818543 - Poiesis Medical, LLC - February 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/poiesis-medical-llc/acf45f02-0c79-42d6-8d79-e912a69d9b9a
Source feed: FDA_Inspections

> FDA Inspection 818543 for Poiesis Medical, LLC on February 12, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818543
- Company Name: Poiesis Medical, LLC
- Inspection Date: 2013-02-12
- 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/poiesis-medical-llc/03a8a2d5-3e29-45b1-9b42-c9df9d88ca8e

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