# FDA Inspection 1049441 - Avent Inc - April 05, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/avent-inc/11527654-92f2-4cbb-a35a-4490bd63a0fd
Source feed: FDA_Inspections

> FDA Inspection 1049441 for Avent Inc on April 05, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1049441
- Company Name: Avent Inc
- Inspection Date: 2018-04-05
- 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 1049441 - 2018-04-05](https://www.globalkeysolutions.net/records/fda_inspections/avent-inc/f505f2f3-e5fc-4b1e-b056-422d3e1c1617)

Company: https://www.globalkeysolutions.net/companies/avent-inc/c68f4e22-e5ce-4baa-85b9-e1eef1bbac69

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