# Imugen, Inc – FDA Inspection, Mar 10, 2017

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

> FDA inspection 1019208 of Imugen, Inc, March 10, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 940432 - 2015-08-26

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)
- Issuing Officer

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