FDA Inspection
Avent, Inc.Avent, Inc. – FDA Inspection, Oct 28, 2016
Record Details
This FDA Inspection record concerns Avent, Inc., with an inspection on October 28, 2016, issued by the Denver District Office, covering medical devices & rad health.
- Company
- Avent, Inc.
- Inspection Date
- October 28, 2016
- Product Type
- Medical Devices & Rad Health
- Office
- Denver District Office
View Company Profile
ID · be8fe316-2223-4c03-8112-adfb3400f61a
Inspection Facts
- Inspection number
- 997411
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Avent, Inc.
11| Date | Classification | Office | Project area |
|---|---|---|---|
| July 10, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 21, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 1, 2017 | Not classified | Denver District Office | |
| August 9, 2017 | Not classified | Denver District Office | |
| November 28, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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 994354 - 2016-11-28
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