# FDA Inspection 969986 - Diamedix Corporation - March 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/diamedix-corporation/5ab07d42-0c65-4b57-a11e-30a080a833bd
Source feed: FDA_Inspections

> FDA Inspection 969986 for Diamedix Corporation on March 17, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969986
- Company Name: Diamedix Corporation
- Inspection Date: 2016-03-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 969986 - 2016-03-17](https://www.keypedia.com/records/fda_inspections/diamedix-corporation/384343a4-2a91-4590-a391-74ba30cec6a2)
- [FDA Inspection 605567 - 2009-08-18](https://www.keypedia.com/records/fda_inspections/diamedix-corporation/bb2cd919-6d5b-451b-958b-a613c71c0961)
- [FDA Inspection 605567 - 2009-08-18](https://www.keypedia.com/records/fda_inspections/diamedix-corporation/a46f037d-67ac-4706-b8ac-89a928d6a8d5)

Company: https://www.keypedia.com/companies/diamedix-corporation/f5b0ed73-8199-4a18-9d68-8785554abb8b

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