# Agiliti Health - Hays – FDA Inspection, Jun 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/agiliti-health-hays/3e8c188e-8442-490f-9bad-02f829d45e4a
Source feed: FDA_Inspections

> FDA inspection 840246 of Agiliti Health - Hays, June 21, 2013. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 840246
- Company Name: Agiliti Health - Hays
- Inspection Date: 2013-06-21
- 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: 5

## Related Documents

- [FDA Inspection 754361 - 2011-11-18](https://www.keypedia.com/records/fda_inspections/agiliti-health-hays/ac5f9b54-7133-4cbe-b35e-6fb186cd4f8c)

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