# FDA Inspection 989444 - Neogen Culture Media - October 07, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/neogen-culture-media/5746515d-f2f8-40d1-9e97-18fb88e86cba
Source feed: FDA_Inspections

> FDA Inspection 989444 for Neogen Culture Media on October 07, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989444
- Company Name: Neogen Culture Media
- Inspection Date: 2016-10-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/neogen-culture-media/05adf193-8de2-4afe-99cf-f25c1d36f24b

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