# FDA Inspection 1180446 - Gentuity, LLC - September 16, 2022

Source: https://www.keypedia.com/records/fda_inspections/gentuity-llc/1f9cd3ce-527d-49ba-843f-1866824ee93f
Source feed: FDA_Inspections

> FDA Inspection 1180446 for Gentuity, LLC on September 16, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180446
- Company Name: Gentuity, LLC
- Inspection Date: 2022-09-16
- 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/gentuity-llc/bc756f97-e3e4-4eac-8be2-9773d64a3f42

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