# FDA Inspection 801766 - Avent, Inc - August 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/avent-inc/21655b5a-d722-4e4e-bb50-3843c14aec47
Source feed: FDA_Inspections

> FDA Inspection 801766 for Avent, Inc on August 23, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 801766
- Company Name: Avent, Inc
- Inspection Date: 2012-08-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 920744 - 2015-04-02](https://www.keypedia.com/records/fda_inspections/avent-inc/8ab22a35-ea33-4a20-9190-c757ff99a422)

Company: https://www.keypedia.com/companies/avent-inc/7469e48b-ef7b-4e45-ade3-2359fad4ea6e

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