# FDA Inspection 1029941 - Ardent, Inc. - October 19, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/ardent-inc/77da0b2a-4716-4f18-94e2-608efdfebd80
Source feed: FDA_Inspections

> FDA Inspection 1029941 for Ardent, Inc. on October 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029941
- Company Name: Ardent, Inc.
- Inspection Date: 2017-10-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029941 - 2017-10-19](https://www.globalkeysolutions.net/records/fda_inspections/ardent-inc/33e871c8-799f-45b0-8fee-7ea748d00858)

Company: https://www.globalkeysolutions.net/companies/ardent-inc/ef78b7fb-d397-4bf7-b38a-49aa243eae0c

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