# FDA Inspection 939204 - Sciton Inc. - August 20, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/sciton-inc/f80d528e-d7be-4509-8b19-af13ee7f4587/
Source feed: FDA_Inspections

> FDA Inspection 939204 for Sciton Inc. on August 20, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939204
- Company Name: Sciton Inc.
- Inspection Date: 2015-08-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 939204 - 2015-08-20](https://www.globalkeysolutions.net/api/records/fda_inspections/sciton-inc/2d8480a8-a893-425d-953b-aa50aaffa924/)
- [FDA Inspection 939204 - 2015-08-20](https://www.globalkeysolutions.net/api/records/fda_inspections/sciton-inc/c1ff2c2d-bf05-4a0d-9f30-0575bd4cdfb4/)
- [FDA Inspection 805362 - 2012-10-25](https://www.globalkeysolutions.net/api/records/fda_inspections/sciton-inc/0a0a71b8-c573-4e41-8537-95240ee46c71/)
- [FDA Inspection 805362 - 2012-10-25](https://www.globalkeysolutions.net/api/records/fda_inspections/sciton-inc/805f3b0d-08e8-43d9-9d6c-6c5c90f1ef8f/)
- [FDA Inspection 652277 - 2010-03-16](https://www.globalkeysolutions.net/api/records/fda_inspections/sciton-inc/3920a3f2-c52f-4fdd-b3d6-024fc8833139/)

Company: https://www.globalkeysolutions.net/companies/sciton-inc/8f629201-23a7-49d5-b8f4-7f1e307e69e0

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