# FDA Inspection 985013 - Creganna Medical Devices - August 18, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/creganna-medical-devices/507c02c3-df92-40b6-80d2-0fa964357409
Source feed: FDA_Inspections

> FDA Inspection 985013 for Creganna Medical Devices on August 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985013
- Company Name: Creganna Medical Devices
- Inspection Date: 2016-08-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 985013 - 2016-08-18](https://www.globalkeysolutions.net/records/fda_inspections/creganna-medical-devices/dab61596-3d9a-4557-810c-11a0e87764dc)

Company: https://www.globalkeysolutions.net/companies/creganna-medical-devices/0019ecd8-5d2d-4c4d-bb31-2a8a5918c673

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