FDA Inspection 620293 — Myotronics-Noromed Inc
The FDA completed an inspection of Myotronics-Noromed Inc on Sep 3, 2009 in Kent, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 3, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kent, WA (United States)