FDA Warning Letter — Euromi S.A.
The FDA took a Warning Letter action against Euromi S.A. on June 22, 2015 (Dison, Belgium). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Euromi S.A.
- Date
- June 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Center
- CDRH
- Location
- Dison (Belgium)