FDA Inspection 737794 — KBD, Inc.
The FDA completed an inspection of KBD, Inc. on July 25, 2011 in North Las Vegas, NV. 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, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- North Las Vegas, NV (United States)