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