FDA Warning Letter — VertiFlex, Inc.
The FDA took a Warning Letter action against VertiFlex, Inc. on July 14, 2010 (Carlsbad, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- VertiFlex, Inc.
- Date
- July 14, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Carlsbad, CA (United States)