# FDA Inspection 1002192 - Penumbra Inc. - February 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/penumbra-inc/1db6d982-aa3a-46c1-ac89-e28f3137708b
Source feed: FDA_Inspections

> FDA Inspection 1002192 for Penumbra Inc. on February 13, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002192
- Company Name: Penumbra Inc.
- Inspection Date: 2017-02-13
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- 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