# Neogen Corporation – FDA Inspection, Mar 13, 2013

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

> FDA inspection 824767 of Neogen Corporation, March 13, 2013. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 969548 - 2016-04-26](https://www.keypedia.com/records/fda_inspections/neogen-corporation/ad1b6c0a-76a0-43cf-87dd-5bb43fa0cb09)
- FDA Inspection 635880 - 2009-12-22

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