# FDA Inspection 754361 - Agiliti Health - Hays - November 18, 2011

Source: https://www.keypedia.com/records/fda_inspections/agiliti-health-hays/ac5f9b54-7133-4cbe-b35e-6fb186cd4f8c
Source feed: FDA_Inspections

> FDA Inspection 754361 for Agiliti Health - Hays on November 18, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 754361
- Company Name: Agiliti Health - Hays
- Inspection Date: 2011-11-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 840246 - 2013-06-21](https://www.keypedia.com/records/fda_inspections/agiliti-health-hays/3e8c188e-8442-490f-9bad-02f829d45e4a)
- [FDA Inspection 754361 - 2011-11-18](https://www.keypedia.com/records/fda_inspections/agiliti-health-hays/2ea69539-b3dc-419e-a41c-69479cb44811)

Company: https://www.keypedia.com/companies/agiliti-health-hays/945f233a-c435-43ee-9d62-e2d7038c54eb

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