# Penumbra Inc. – FDA Inspection, Aug 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/penumbra-inc/0eb85d66-83fd-4f57-8ac0-e84940f07d44
Source feed: FDA_Inspections

> FDA inspection 614070 of Penumbra Inc., August 28, 2009. Classification: Official Action Indicated (OAI). 8 citations under 21 CFR parts 803 and 820. 10 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 614070
- Company Name: Penumbra Inc.
- Inspection Date: 2009-08-28
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## 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 965001 - 2016-02-23](https://www.keypedia.com/records/fda_inspections/penumbra-inc/8946649a-6efd-460d-ba42-079ec87daccd)
- [FDA Inspection 936229 - 2015-08-04](https://www.keypedia.com/records/fda_inspections/penumbra-inc/953eae88-8bf3-44dc-a358-663fdbf723dd)

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