# FDA Inspection 1091806 - Clariance Inc - June 04, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/clariance-inc/fce3ec09-e267-4696-b661-2a9e0b902e65/
Source feed: FDA_Inspections

> FDA Inspection 1091806 for Clariance Inc on June 04, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1091806
- Company Name: Clariance Inc
- Inspection Date: 2019-06-04
- 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 1091806 - 2019-06-04](https://www.globalkeysolutions.net/api/records/fda_inspections/clariance-inc/45dd7cc3-d1ef-46b4-ae7d-516651cb71ff/)
- [FDA Inspection 885453 - 2014-06-30](https://www.globalkeysolutions.net/api/records/fda_inspections/clariance-inc/f827d903-be8b-4c39-a096-eb91cadfef7d/)
- [FDA Inspection 885453 - 2014-06-30](https://www.globalkeysolutions.net/api/records/fda_inspections/clariance-inc/e69db775-3a1f-4b7a-bd08-860009fd34a8/)

Company: https://www.globalkeysolutions.net/companies/clariance-inc/c3508c94-08ec-470f-8c29-c60291a76771

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