FDA Inspection 708055 — Bionetek Corporation
The FDA completed an inspection of Bionetek Corporation on Jan 27, 2011 in El Monte, CA. 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
- Jan 27, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- El Monte, CA (United States)