# FDA Inspection 901658 - ClearLine MD - October 29, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearline-md/9c14675a-616f-46e8-9af6-4132ee4294ca
Source feed: FDA_Inspections

> FDA Inspection 901658 for ClearLine MD on October 29, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901658
- Company Name: ClearLine MD
- Inspection Date: 2014-10-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1042336 - 2018-02-08](https://www.globalkeysolutions.net/records/fda_inspections/clearline-md/237cd862-9508-4d97-a6b0-acbbecd4a025)

Company: https://www.globalkeysolutions.net/companies/clearline-md/8a01c6de-6226-43e7-bc13-91ccaa0454f6

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