FDA Warning Letter — Penumbra Inc.
The FDA took a Warning Letter action against Penumbra Inc. on December 31, 2009 (Alameda, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Penumbra Inc.
- Date
- December 31, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Alameda, CA (United States)