FDA Warning Letter — TELEMED
The FDA took a Warning Letter action against TELEMED on November 14, 2017 (Vilnius, Lithuania). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.
Action Details
- Facility
- TELEMED
- Date
- November 14, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Center
- CDRH
- Location
- Vilnius (Lithuania)