# FDA Inspection 669723 - R.P. Kincheloe dba Perkins Healthcare Technologies - June 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/rp-kincheloe-dba-perkins-healthcare-technologies/e6b90817-d594-45b2-83b7-3d14441fd587
Source feed: FDA_Inspections

> FDA Inspection 669723 for R.P. Kincheloe dba Perkins Healthcare Technologies on June 29, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 669723
- Company Name: R.P. Kincheloe dba Perkins Healthcare Technologies
- Inspection Date: 2010-06-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 669723 - 2010-06-29](https://www.keypedia.com/records/fda_inspections/rp-kincheloe-dba-perkins-healthcare-technologies/a6d3826c-d7c7-442f-9527-eadaa4fb0071)

Company: https://www.keypedia.com/companies/rp-kincheloe-dba-perkins-healthcare-technologies/b5ab1899-b278-4a4c-b66c-8750edc39e7e

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