FDA Warning Letter — QLRAD
The FDA took a Warning Letter action against QLRAD on Jul 20, 2017 (Almere, Netherlands). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- QLRAD
- Date
- Jul 20, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Center
- CDRH
- Location
- Almere (Netherlands)