FDA Warning Letter — LumiQuick Diagnostics Inc.
The FDA took a Warning Letter action against LumiQuick Diagnostics Inc. on April 1, 2014 (Santa Clara, 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
- LumiQuick Diagnostics Inc.
- Date
- April 1, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Center
- CDRH
- Location
- Santa Clara, CA (United States)