# FDA Inspection 756449 - HistoGeneX - October 28, 2011

Source: https://www.keypedia.com/records/fda_inspections/histogenex/ac2e80bd-e0e8-4c94-a293-9ee6c4ad0c90
Source feed: FDA_Inspections

> FDA Inspection 756449 for HistoGeneX on October 28, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 756449
- Company Name: HistoGeneX
- Inspection Date: 2011-10-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/histogenex/99ac74af-fc42-4dfc-9f02-37709f02662a

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