# FDA Inspection 839722 - The Kilroy Company - July 10, 2011

Source: https://www.keypedia.com/records/fda_inspections/the-kilroy-company/3bfba629-58c6-48c7-9d71-44789cf99712
Source feed: FDA_Inspections

> FDA Inspection 839722 for The Kilroy Company on July 10, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839722
- Company Name: The Kilroy Company
- Inspection Date: 2011-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/the-kilroy-company/6c49b0b6-1612-4b03-bbec-25be2cc73975

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