# FDA Inspection 614070 - Penumbra Inc. - August 28, 2009

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

> FDA Inspection 614070 for Penumbra Inc. on August 28, 2009. Classification: Official Action Indicated (OAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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