FDA Inspection 808640 — Arrowhead DE LLC

Arrowhead DE LLC — FEI 3008817603

The FDA completed an inspection of Arrowhead DE LLC on November 20, 2012 in Peachtree City, GA. 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
November 20, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Peachtree City, GA (United States)