# FDA Inspection 1019208 - Imugen, Inc - March 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/imugen-inc/a5aee14d-f3be-4592-9f58-3bf2ff8b6f31
Source feed: FDA_Inspections

> FDA Inspection 1019208 for Imugen, Inc on March 10, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019208
- Company Name: Imugen, Inc
- Inspection Date: 2017-03-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 940432 - 2015-08-26](https://www.keypedia.com/records/fda_inspections/imugen-inc/70a59277-a006-4737-98d3-612e0ac6fdf5)

Company: https://www.keypedia.com/companies/imugen-inc/93bd988a-b9ee-4eef-bb6e-2a00613de8a6

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