# FDA Inspection 1007159 - Colonic Plus - December 06, 2016

Source: https://www.keypedia.com/records/fda_inspections/colonic-plus/acdf56a8-ae7f-4179-b5c4-041cf856e614
Source feed: FDA_Inspections

> FDA Inspection 1007159 for Colonic Plus on December 06, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007159
- Company Name: Colonic Plus
- Inspection Date: 2016-12-06
- 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 1007159 - 2016-12-06](https://www.keypedia.com/records/fda_inspections/colonic-plus/49f00737-1961-464c-a2a1-bbdf655b2d84)

Company: https://www.keypedia.com/companies/colonic-plus/51ac273b-0070-4d4e-9cc0-0b2124aade9c

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