FDA Inspection 1020669 — Kwivik Medical, Inc.
The FDA completed an inspection of Kwivik Medical, Inc. on July 25, 2017 in Frisco, TX. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- July 25, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Frisco, TX (United States)