# FDA Inspection 901256 - ClearFlow Inc. - October 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/clearflow-inc/7e76e8e6-88f6-4414-a134-a2ab996e2b9a
Source feed: FDA_Inspections

> FDA Inspection 901256 for ClearFlow Inc. on October 17, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901256
- Company Name: ClearFlow Inc.
- Inspection Date: 2014-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 901256 - 2014-10-17](https://www.keypedia.com/records/fda_inspections/clearflow-inc/7eb9cc04-d617-4099-aef5-13b9a4be9e58)

Company: https://www.keypedia.com/companies/clearflow-inc/329ba605-d19d-492b-be3d-979886cdf401

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