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FDA Inspection
•Avent, Inc.•November 28, 2016

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

Record Details

This FDA Inspection record concerns Avent, Inc., with an inspection on November 28, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Avent, Inc.
Inspection Date
November 28, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Janet Pulver (FDA Associated Person)
View Company Profile

ID · aa54d4b7-74b6-4346-aed5-368e03779c9f

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
994354
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Avent, Inc.

11
DateClassificationOfficeProject area
July 10, 2025NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 21, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 1, 2017Not classifiedDenver District Office
August 9, 2017Not classifiedDenver District Office
October 28, 2016Not classifiedDenver District Office
View all 11 other inspections on the company page
Other documents for Avent, Inc.
  • FDA Inspection 1275741 - 2025-07-10
  • FDA Inspection 1118646 - 2020-02-21
  • FDA Inspection 1089505 - 2017-12-01
  • FDA Inspection 1037129 - 2017-08-09
  • FDA Inspection 997411 - 2016-10-28

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