# FDA Inspection 889005 - Interrad Medical Inc - July 31, 2014

Source: https://www.keypedia.com/records/fda_inspections/interrad-medical-inc/23d9f7a4-2432-4b66-904f-a3766f6b3f3e
Source feed: FDA_Inspections

> FDA Inspection 889005 for Interrad Medical Inc on July 31, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 889005
- Company Name: Interrad Medical Inc
- Inspection Date: 2014-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 699977 - 2010-11-05](https://www.keypedia.com/records/fda_inspections/interrad-medical-inc/b44f380c-b30f-4324-9ed0-583ae5004719)

Company: https://www.keypedia.com/companies/interrad-medical-inc/1d41298b-4a9b-44d9-80ad-ea3c8e827a70

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