FDA Inspection 750110 — Collimare, LLC
The FDA completed an inspection of Collimare, LLC on September 30, 2011 in Golden, CO. 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
- September 30, 2011
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Golden, CO (United States)