FDA Warning Letter — KBD, Inc.
The FDA took a Warning Letter action against KBD, Inc. on December 15, 2011 (North Las Vegas, NV). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.
Action Details
- Facility
- KBD, Inc.
- Date
- December 15, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Center
- CDRH
- Location
- North Las Vegas, NV (United States)