# The Kilroy Company – FDA Inspection, Jan 7, 2009

Source: https://www.keypedia.com/records/fda_inspections/the-kilroy-company/c382f12c-e12a-49d0-8cb4-fcbb13fb3800
Source feed: FDA_Inspections

> FDA inspection 538058 of The Kilroy Company, January 07, 2009. Classification: Voluntary Action Indicated (VAI). 34 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 538058
- Company Name: The Kilroy Company
- Inspection Date: 2009-01-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 34

## Related Documents

- FDA Inspection 839722 - 2011-07-10
- [FDA Inspection 606924 - 2009-09-11](https://www.keypedia.com/records/fda_inspections/the-kilroy-company/93ed0cab-5f08-4b33-af24-cb49409e4a7b)

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