# FDA Inspection 1094620 - Orthogen Corporation - April 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/orthogen-corporation/fc723a16-c672-4b03-a3ac-0174b57dd95a
Source feed: FDA_Inspections

> FDA Inspection 1094620 for Orthogen Corporation on April 10, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094620
- Company Name: Orthogen Corporation
- Inspection Date: 2019-04-10
- 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/orthogen-corporation/983063b9-88b5-4ede-a78d-f99d36e0a740

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