FDA Inspection 979231 — Abiomed Europe GmbH
The FDA completed an inspection of Abiomed Europe GmbH on Jun 23, 2016 in Aachen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 23, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Aachen (Germany)
Additional Details
Postmarket Audit Inspections