FDA Inspection 665312 — Elekta Inc
The FDA completed an inspection of Elekta Inc on May 14, 2010 in Saint Charles, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 14, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Saint Charles, MO (United States)