FDA Warning Letter — Spes Medica Srl
The FDA took a Warning Letter action against Spes Medica Srl on Jan 23, 2013 (Battipaglia, Italy). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action details
- Facility
- Spes Medica Srl
- Date
- Jan 23, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Center
- CDRH
- Location
- Battipaglia (Italy)