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FDA Inspection 965001 — Penumbra Inc.

Penumbra Inc. — FEI 3005168196

The FDA completed an inspection of Penumbra Inc. on February 23, 2016 in Alameda, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 23, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Alameda, CA (United States)

Facility

Other inspections at this facility

  • 1145527 (NAI Mon Jun 21 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1002192 (NAI Mon Feb 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 936229 (NAI Tue Aug 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 938074 (VAI Wed Jul 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876601 (NAI Wed Apr 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources