# Avent, Inc. – FDA Inspection, Nov 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/avent-inc/aa54d4b7-74b6-4346-aed5-368e03779c9f
Source feed: FDA_Inspections

> FDA inspection 994354 of Avent, Inc., November 28, 2016. Classification: No Action Indicated (NAI). 11 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 994354
- Company Name: Avent, Inc.
- Inspection Date: 2016-11-28
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1275741 - 2025-07-10
- [FDA Inspection 1118646 - 2020-02-21](https://www.keypedia.com/records/fda_inspections/avent-inc/3f3dcf60-84c0-4d69-a334-9fd0019a8435)
- FDA Inspection 1089505 - 2017-12-01
- FDA Inspection 1037129 - 2017-08-09
- [FDA Inspection 997411 - 2016-10-28](https://www.keypedia.com/records/fda_inspections/avent-inc/be8fe316-2223-4c03-8112-adfb3400f61a)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/janet-pulver/d46b01cd-8c3d-4a54-bb91-843e0f94de89)

Company: https://www.keypedia.com/companies/avent-inc/f7d3c6c2-23e3-480a-a54d-56949ec4b1da

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