FDA Inspection 997378 — DNA Genotek Inc.
The FDA completed an inspection of DNA Genotek Inc. on Nov 3, 2016 in Kanata. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 3, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kanata (Canada)