FDA Inspection 851753 — DNA Genotek Inc.
The FDA completed an inspection of DNA Genotek Inc. on Sep 20, 2013 in Kanata. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Sep 20, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kanata (Canada)