# FDA Inspection 769596 - Penumbra Inc. - February 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/penumbra-inc/c21ee4bc-37b2-44d8-85cb-d7d842e4525d
Source feed: FDA_Inspections

> FDA Inspection 769596 for Penumbra Inc. on February 27, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 769596
- Company Name: Penumbra Inc.
- Inspection Date: 2012-02-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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