# FDA Inspection 1216536 - Entrogen, Inc - July 31, 2023

Source: https://www.keypedia.com/records/fda_inspections/entrogen-inc/887384e1-5857-433e-8c04-b2bba6292cbe
Source feed: FDA_Inspections

> FDA Inspection 1216536 for Entrogen, Inc on July 31, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216536
- Company Name: Entrogen, Inc
- Inspection Date: 2023-07-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/entrogen-inc/ef3ad92b-673a-4835-aad2-55f22a9a2aeb

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