# FDA Inspection 824767 - Neogen Corporation - March 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/neogen-corporation/aeaca107-9403-4e1c-a5e0-e60792917790
Source feed: FDA_Inspections

> FDA Inspection 824767 for Neogen Corporation on March 13, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824767
- Company Name: Neogen Corporation
- Inspection Date: 2013-03-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/neogen-corporation/afccf2bd-cd1e-4b1a-8f84-82d1584f86ac

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