FDA Warning Letter — Rubimed AG
The FDA took a Warning Letter action against Rubimed AG on May 6, 2013 (Hergiswil Nw, Switzerland). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- Rubimed AG
- Date
- May 6, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Hergiswil Nw (Switzerland)