# FDA Inspection 907529 - CompleWare Corporation - December 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/compleware-corporation/3e62b276-992b-4e7c-ae09-4009d61074b8
Source feed: FDA_Inspections

> FDA Inspection 907529 for CompleWare Corporation on December 18, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907529
- Company Name: CompleWare Corporation
- Inspection Date: 2014-12-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 907529 - 2014-12-18](https://www.keypedia.com/records/fda_inspections/compleware-corporation/0cb8d8de-27df-497c-8847-e8c28dcb2d64)

Company: https://www.keypedia.com/companies/compleware-corporation/d390bf7c-9b6f-41ad-ad57-98eef4271015

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