# FDA Inspection 958232 - Cartiva, Inc - January 20, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/cartiva-inc/9f3f6bb7-8f4c-4479-a131-c0d97720ed27
Source feed: FDA_Inspections

> FDA Inspection 958232 for Cartiva, Inc on January 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 958232
- Company Name: Cartiva, Inc
- Inspection Date: 2016-01-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1032140 - 2017-10-30](https://www.globalkeysolutions.net/records/fda_inspections/cartiva-inc/95eab92a-9486-4917-b86d-ec1f93434c09)
- [FDA Inspection 958232 - 2016-01-20](https://www.globalkeysolutions.net/records/fda_inspections/cartiva-inc/6910b42b-81ed-46b2-aab8-7a95d5b2ad63)

Company: https://www.globalkeysolutions.net/companies/cartiva-inc/2798c157-21b3-41b5-92f0-e60bc59d4677

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