# The Kilroy Company – FDA Inspection, Sep 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/the-kilroy-company/93ed0cab-5f08-4b33-af24-cb49409e4a7b
Source feed: FDA_Inspections

> FDA inspection 606924 of The Kilroy Company, September 11, 2009. Classification: Voluntary Action Indicated (VAI). 17 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 606924
- Company Name: The Kilroy Company
- Inspection Date: 2009-09-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 17

## Related Documents

- FDA Inspection 839722 - 2011-07-10
- [FDA Inspection 538058 - 2009-01-07](https://www.keypedia.com/records/fda_inspections/the-kilroy-company/c382f12c-e12a-49d0-8cb4-fcbb13fb3800)

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