FDA Warning Letter — Eidosmed
The FDA took a Warning Letter action against Eidosmed on Mar 16, 2011 (Chicago, IL). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- Eidosmed
- Date
- Mar 16, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Center
- CDRH
- Location
- Chicago, IL (United States)