# FDA Inspection 632743 - Kerr Corporation - December 07, 2009

Source: https://www.keypedia.com/records/fda_inspections/kerr-corporation/5f792093-8b14-4fe9-b6a8-0be123704e87
Source feed: FDA_Inspections

> FDA Inspection 632743 for Kerr Corporation on December 07, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 632743
- Company Name: Kerr Corporation
- Inspection Date: 2009-12-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 752891 - 2011-11-08](https://www.keypedia.com/records/fda_inspections/kerr-corporation/02772ed4-c534-4297-ba6e-f8de069a55ab)
- [FDA Inspection 752891 - 2011-11-08](https://www.keypedia.com/records/fda_inspections/kerr-corporation/388175f7-3194-40ee-a6ce-f34c44a1d242)
- [FDA Inspection 632743 - 2009-12-07](https://www.keypedia.com/records/fda_inspections/kerr-corporation/d6900772-928b-492e-a59a-97496099c5e1)

Company: https://www.keypedia.com/companies/kerr-corporation/ceab5f8b-1ef2-4abc-8fef-419c074c12c2

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