# FDA Inspection 821939 - Kerr Corporation - March 08, 2013

Source: https://www.keypedia.com/records/fda_inspections/kerr-corporation/1d9be4d0-efe2-4041-92ef-4b3fc8020990
Source feed: FDA_Inspections

> FDA Inspection 821939 for Kerr Corporation on March 08, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821939
- Company Name: Kerr Corporation
- Inspection Date: 2013-03-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 821939 - 2013-03-08](https://www.keypedia.com/records/fda_inspections/kerr-corporation/cb442b7c-f6d9-4a9b-9d33-1c5d53972fa0)
- [FDA Inspection 648590 - 2010-02-18](https://www.keypedia.com/records/fda_inspections/kerr-corporation/38852978-d883-4153-9c68-17a086d677d1)
- [FDA Inspection 648590 - 2010-02-18](https://www.keypedia.com/records/fda_inspections/kerr-corporation/19fc4dc8-2975-44ec-b998-a390bbff6496)

Company: https://www.keypedia.com/companies/kerr-corporation/67efac13-c7b5-4c88-b109-07723434077e

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