# FDA Inspection 967762 - Nephros, Inc. - February 22, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/nephros-inc/0ec9d868-932d-46cd-9d61-35d8b558d97b
Source feed: FDA_Inspections

> FDA Inspection 967762 for Nephros, Inc. on February 22, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 967762
- Company Name: Nephros, Inc.
- Inspection Date: 2016-02-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 967762 - 2016-02-22](https://www.globalkeysolutions.net/records/fda_inspections/nephros-inc/d42c1dd4-714a-4423-b9d1-ecd125225941)
- [FDA Inspection 905362 - 2014-10-24](https://www.globalkeysolutions.net/records/fda_inspections/nephros-inc/18713c93-0a4a-48fa-9ee3-62660887809f)
- [FDA Inspection 905362 - 2014-10-24](https://www.globalkeysolutions.net/records/fda_inspections/nephros-inc/7a9348ea-3c89-431f-95b1-dc06fea0b866)
- [FDA Inspection 851457 - 2013-11-13](https://www.globalkeysolutions.net/records/fda_inspections/nephros-inc/2d3390ec-f6a4-4488-85a5-88f0b734cdcd)

Company: https://www.globalkeysolutions.net/companies/nephros-inc/748317fb-e75e-45ff-8356-313d1a1efaed

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