FDA Inspection 1002192 — Penumbra Inc.
The FDA completed an inspection of Penumbra Inc. on February 13, 2017 in Alameda, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 13, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Alameda, CA (United States)
Additional Details
Clinical Investigator (CI)