# FDA Inspection 1100501 - Agiliti Health Inc. - August 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/agiliti-health-inc/93aa2a94-a3ae-43e4-af38-af3c8fc32b48
Source feed: FDA_Inspections

> FDA Inspection 1100501 for Agiliti Health Inc. on August 27, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100501
- Company Name: Agiliti Health Inc.
- Inspection Date: 2019-08-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100501 - 2019-08-27](https://www.keypedia.com/records/fda_inspections/agiliti-health-inc/08a59c37-d118-4138-b851-bb45d5b63dc7)

Company: https://www.keypedia.com/companies/agiliti-health-inc/e038ef15-0333-4ff1-b614-8291b6b7cc3e

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