# FDA Inspection 1091600 - Theragen, Inc - May 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/theragen-inc/4fbdacdd-c5e5-40fd-8f86-e8d7cfcfa08d
Source feed: FDA_Inspections

> FDA Inspection 1091600 for Theragen, Inc on May 23, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091600
- Company Name: Theragen, Inc
- Inspection Date: 2019-05-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/theragen-inc/68912441-b041-4b0f-8fa4-222e1f67b85a

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