# FDA Inspection 598806 - KHL Inc - July 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/khl-inc/0a47458c-7da7-466c-b0da-219594be1559
Source feed: FDA_Inspections

> FDA Inspection 598806 for KHL Inc on July 14, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598806
- Company Name: KHL Inc
- Inspection Date: 2009-07-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/khl-inc/6190dad8-9f82-477a-b96d-0232a9251808

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