FDA Inspection
Microvention, Inc.Microvention, Inc. – FDA Inspection, Aug 25, 2016
Record Details
This FDA Inspection record concerns Microvention, Inc., with an inspection on August 25, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Microvention, Inc.
- Inspection Date
- August 25, 2016
- Product Type
- Devices
View Company Profile
ID · 949bee0e-b5c6-420d-85a9-f6a2085cae31
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 986764
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Microvention, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 8, 2025 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| May 24, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 28, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 30, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 20, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Microvention, Inc.
- FDA Inspection 1258987 - 2025-01-08
- FDA Inspection 1153926 - 2021-05-24
- FDA Inspection 915040 - 2015-01-28
- FDA Inspection 830029 - 2013-04-30
- FDA Inspection 629675 - 2009-11-20
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.