FDA Warning Letter — Prodimed
The FDA took a Warning Letter action against Prodimed on Nov 2, 2015 (Neuilly En Thelle, France). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.
Action details
- Facility
- Prodimed
- Date
- Nov 2, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Center
- CDRH
- Location
- Neuilly En Thelle (France)