FDA Warning Letter — Neoventa Medical AB
The FDA took a Warning Letter action against Neoventa Medical AB on August 4, 2010 (Molndal, Sweden). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.
Action Details
- Facility
- Neoventa Medical AB
- Date
- August 4, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- Molndal (Sweden)