# FDA Inspection 650133 - Kayline Inc - March 05, 2010

Source: https://www.keypedia.com/records/fda_inspections/kayline-inc/3464a332-66b6-459d-9328-7b1029abdbb5
Source feed: FDA_Inspections

> FDA Inspection 650133 for Kayline Inc on March 05, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 650133
- Company Name: Kayline Inc
- Inspection Date: 2010-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 756827 - 2011-12-08](https://www.keypedia.com/records/fda_inspections/kayline-inc/92e168ba-702a-4cc4-b1e2-50e20967f163)

Company: https://www.keypedia.com/companies/kayline-inc/a44fd1c7-be8e-4416-82f3-cb69913c94db

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