# Kerr Corporation – FDA Inspection, Mar 8, 2013

Source: https://www.keypedia.com/records/fda_inspections/kerr-corporation/cb442b7c-f6d9-4a9b-9d33-1c5d53972fa0
Source feed: FDA_Inspections

> FDA inspection 821939 of Kerr Corporation, March 08, 2013. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821939
- Company Name: Kerr Corporation
- Inspection Date: 2013-03-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1122113 - 2018-10-04](https://www.keypedia.com/records/fda_inspections/kerr-corporation/91dd66ea-f0a2-4afb-ba5d-80a7b17f835c)
- [FDA Inspection 1030505 - 2017-05-03](https://www.keypedia.com/records/fda_inspections/kerr-corporation/0ab6927e-5afb-4827-aa1c-bd02fdd1468a)
- [FDA Inspection 648590 - 2010-02-18](https://www.keypedia.com/records/fda_inspections/kerr-corporation/38852978-d883-4153-9c68-17a086d677d1)

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
