FDA Warning Letter — Myotronics-Noromed Inc
The FDA took a Warning Letter action against Myotronics-Noromed Inc on Apr 9, 2012 (Kent, WA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.
Action Details
- Facility
- Myotronics-Noromed Inc
- Date
- Apr 9, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Center
- CDRH
- Location
- Kent, WA (United States)