# FDA Inspection 985877 - Unilife Medical Solutions, Inc. - August 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/unilife-medical-solutions-inc/00f0fccf-ce65-4df2-8202-1b19a42edde6
Source feed: FDA_Inspections

> FDA Inspection 985877 for Unilife Medical Solutions, Inc. on August 30, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985877
- Company Name: Unilife Medical Solutions, Inc.
- Inspection Date: 2016-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 834576 - 2013-04-19](https://www.keypedia.com/records/fda_inspections/unilife-medical-solutions-inc/b870b352-e04c-4d5c-90c9-c4fc85687a20)

Company: https://www.keypedia.com/companies/unilife-medical-solutions-inc/2fef8753-4c27-44f8-8215-79b4e49363b1

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