FDA Warning Letter — Arjo Inc.

Case 419751 — FEI 3009988881

The FDA took a Warning Letter action against Arjo Inc. on September 18, 2014 (San Antonio, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Arjo Inc.
Date
September 18, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
San Antonio, TX (United States)