# FDA Inspection 913137 - Sckoon, Inc. - February 09, 2015

Source: https://www.keypedia.com/records/fda_inspections/sckoon-inc/f6521abc-c2b2-4dc9-9e49-c45b269c6966
Source feed: FDA_Inspections

> FDA Inspection 913137 for Sckoon, Inc. on February 09, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 913137
- Company Name: Sckoon, Inc.
- Inspection Date: 2015-02-09
- 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 913137 - 2015-02-09](https://www.keypedia.com/records/fda_inspections/sckoon-inc/1b438fae-fdfa-471e-b83c-d9eef6cfab81)

Company: https://www.keypedia.com/companies/sckoon-inc/b284a4ab-7af0-4d2d-ba2c-baaf26e74542

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