FDA Inspection
Penumbra Inc.Penumbra Inc. – FDA Inspection, Feb 27, 2012
Record Details
This FDA Inspection record concerns Penumbra Inc., with an inspection on February 27, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Penumbra Inc.
- Inspection Date
- February 27, 2012
- Product Type
- Devices
View Company Profile
ID · c21ee4bc-37b2-44d8-85cb-d7d842e4525d
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 769596
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Penumbra Inc.
10| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 13, 2018 | Not classified | San Francisco District Office | |
| February 13, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 23, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 4, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Penumbra Inc.
- FDA Inspection 1145527 - 2021-06-21
- FDA Inspection 1065797 - 2018-06-13
- FDA Inspection 1002192 - 2017-02-13
- FDA Inspection 965001 - 2016-02-23
- FDA Inspection 936229 - 2015-08-04
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