FDA Inspection
Imugen, IncImugen, Inc – FDA Inspection, Mar 10, 2017
Record Details
This FDA Inspection record concerns Imugen, Inc, with an inspection on March 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- People
- Justine M. Corson (FDA Associated Person)
- Lori P. Peters (Issuing Officer)
View Company Profile
ID · a5aee14d-f3be-4592-9f58-3bf2ff8b6f31
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019208
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Imugen, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 26, 2015 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
Other documents for Imugen, Inc
- FDA Inspection 940432 - 2015-08-26
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