FDA Warning Letter — Advanced OrthoPro, Inc.

Case 307439 — FEI 3007912159

The FDA took a Warning Letter action against Advanced OrthoPro, Inc. on May 18, 2012 (Indianapolis, IN). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Advanced OrthoPro, Inc.
Date
May 18, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Indianapolis, IN (United States)