# FDA Inspection 1038629 - Shift Labs Inc - January 25, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/shift-labs-inc/234d25f6-8e4f-41e3-abb8-12a8a37ba629
Source feed: FDA_Inspections

> FDA Inspection 1038629 for Shift Labs Inc on January 25, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038629
- Company Name: Shift Labs Inc
- Inspection Date: 2018-01-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1038629 - 2018-01-25](https://www.globalkeysolutions.net/records/fda_inspections/shift-labs-inc/6d31f2d8-2240-4000-ad0d-bb50709fa668)

Company: https://www.globalkeysolutions.net/companies/shift-labs-inc/9d8f2ad8-cb6b-47dd-ae8e-103dfbabca85

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