# FDA Inspection 1042336 - ClearLine MD - February 08, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearline-md/237cd862-9508-4d97-a6b0-acbbecd4a025
Source feed: FDA_Inspections

> FDA Inspection 1042336 for ClearLine MD on February 08, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1042336
- Company Name: ClearLine MD
- Inspection Date: 2018-02-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 901658 - 2014-10-29](https://www.globalkeysolutions.net/records/fda_inspections/clearline-md/9c14675a-616f-46e8-9af6-4132ee4294ca)

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