FDA Inspection
Penumbra Inc.Penumbra Inc. – FDA Inspection, Jun 13, 2018
Record Details
This FDA Inspection record concerns Penumbra Inc., with an inspection on June 13, 2018, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Penumbra Inc.
- Inspection Date
- June 13, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 8f48c09d-d07c-43bc-8b5b-e2358b2b7b9b
Inspection Facts
- Inspection number
- 1065797
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 |
| 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 |
| July 15, 2015 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Penumbra Inc.
- FDA Inspection 1145527 - 2021-06-21
- FDA Inspection 1002192 - 2017-02-13
- FDA Inspection 965001 - 2016-02-23
- FDA Inspection 936229 - 2015-08-04
- FDA Inspection 938074 - 2015-07-15
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