# FDA Inspection 985208 - Cianna Medical, Inc. - September 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/cianna-medical-inc/feaffb99-e3c5-4aa9-ad84-93d1a25e5dcf
Source feed: FDA_Inspections

> FDA Inspection 985208 for Cianna Medical, Inc. on September 09, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985208
- Company Name: Cianna Medical, Inc.
- Inspection Date: 2016-09-09
- 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 985208 - 2016-09-09](https://www.keypedia.com/records/fda_inspections/cianna-medical-inc/4027e083-beaf-43ff-b085-8e197a8e56b9)
- [FDA Inspection 762316 - 2012-01-09](https://www.keypedia.com/records/fda_inspections/cianna-medical-inc/e59acee5-82f4-4251-8743-8643ca65fbb4)
- [FDA Inspection 762316 - 2012-01-09](https://www.keypedia.com/records/fda_inspections/cianna-medical-inc/029beee0-fb2c-47c2-b5b7-7d83c834ae49)

Company: https://www.keypedia.com/companies/cianna-medical-inc/ecd59544-4634-4535-9cb7-83f1efbe4414

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