FDA Inspection 768810 — Arrowhead DE LLC

Arrowhead DE LLC — FEI 3008817603

The FDA completed an inspection of Arrowhead DE LLC on February 21, 2012 in Peachtree City, GA. 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
February 21, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Peachtree City, GA (United States)