# FDA Inspection 1020669 - Kwivik Medical, Inc. - July 25, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/kwivik-medical-inc/fe4bd546-db58-46c1-beb8-29353fee6def/
Source feed: FDA_Inspections

> FDA Inspection 1020669 for Kwivik Medical, Inc. on July 25, 2017. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1020669
- Company Name: Kwivik Medical, Inc.
- Inspection Date: 2017-07-25
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1040026 - 2017-12-12](https://www.globalkeysolutions.net/api/records/fda_inspections/kwivik-medical-inc/21b5fa43-551c-4fb3-a219-75595a2e0315/)
- [FDA Inspection 1020669 - 2017-07-25](https://www.globalkeysolutions.net/api/records/fda_inspections/kwivik-medical-inc/3a95fe3f-bec8-47f4-85d2-774d6b5dd486/)

Company: https://www.globalkeysolutions.net/companies/kwivik-medical-inc/fda120b8-2bc9-42d3-821d-2170b9e50b3a

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