FDA Inspection 772239 — AllMed Systems Inc.
The FDA completed an inspection of AllMed Systems Inc. on February 15, 2012 in Livermore, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 15, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Livermore, CA (United States)