FDA Inspection 1040026 — Kwivik Medical, Inc.
The FDA completed an inspection of Kwivik Medical, Inc. on Dec 12, 2017 in Frisco, TX. 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
- Dec 12, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Frisco, TX (United States)