# FDA Inspection 667224 - Kustomer Kinetics, Inc. - June 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/kustomer-kinetics-inc/b6fad854-c5a0-443f-a08d-00a369f1481b
Source feed: FDA_Inspections

> FDA Inspection 667224 for Kustomer Kinetics, Inc. on June 15, 2010. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 667224
- Company Name: Kustomer Kinetics, Inc.
- Inspection Date: 2010-06-15
- 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 667224 - 2010-06-15](https://www.keypedia.com/records/fda_inspections/kustomer-kinetics-inc/83583f43-1ab4-4578-87dc-b8e79cb7af49)

Company: https://www.keypedia.com/companies/kustomer-kinetics-inc/42d3ff41-14ea-4485-a230-ff7bfe31b72f

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