# Penumbra Inc. – FDA Inspection, Feb 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/penumbra-inc/8946649a-6efd-460d-ba42-079ec87daccd
Source feed: FDA_Inspections

> FDA inspection 965001 of Penumbra Inc., February 23, 2016. Classification: Voluntary Action Indicated (VAI). 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965001
- Company Name: Penumbra Inc.
- Inspection Date: 2016-02-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1145527 - 2021-06-21
- [FDA Inspection 1065797 - 2018-06-13](https://www.keypedia.com/records/fda_inspections/penumbra-inc/8f48c09d-d07c-43bc-8b5b-e2358b2b7b9b)
- FDA Inspection 1002192 - 2017-02-13
- [FDA Inspection 936229 - 2015-08-04](https://www.keypedia.com/records/fda_inspections/penumbra-inc/953eae88-8bf3-44dc-a358-663fdbf723dd)
- [FDA Inspection 938074 - 2015-07-15](https://www.keypedia.com/records/fda_inspections/penumbra-inc/099b3766-015b-4227-9d31-1f79ee21df00)

Company: https://www.keypedia.com/companies/penumbra-inc/8b3e95a4-a5b1-40f4-9baf-8dfc5e2d64e4

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7