FDA Inspection 791995 — CoRE labs, LLC

CoRE labs, LLC — FEI 3001620005

The FDA completed an inspection of CoRE labs, LLC on July 25, 2012 in Englewood, CO. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 25, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Englewood, CO (United States)