FDA Warning Letter — Arrowhead DE LLC

Case 301261 — FEI 3008817603

The FDA took a Warning Letter action against Arrowhead DE LLC on May 18, 2012 (Peachtree City, GA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Arrowhead DE LLC
Date
May 18, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Peachtree City, GA (United States)