FDA Inspection 1021587 — Abiomed, Inc.
The FDA completed an inspection of Abiomed, Inc. on July 27, 2017 in Danvers, MA. 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
- July 27, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Danvers, MA (United States)
Additional Details
Sponsor, Contract Research Organization