FDA Inspection 555085 — Collimare, LLC
The FDA completed an inspection of Collimare, LLC on December 9, 2008 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
- December 9, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Golden, CO (United States)