FDA Warning Letter — Helica Instruments, Ltd.
The FDA took a Warning Letter action against Helica Instruments, Ltd. on May 13, 2016 (Edinburgh, United Kingdom). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- Helica Instruments, Ltd.
- Date
- May 13, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Center
- CDRH
- Location
- Edinburgh (United Kingdom)