FDA Inspection 1011040 — Prollenium Medical Technologies Inc.
The FDA completed an inspection of Prollenium Medical Technologies Inc. on Apr 20, 2017 in Aurora. 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
- Apr 20, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Aurora (Canada)
Additional details
Sponsor, Contract Research Organization